A 60-Year Tale of Spots, Maps, and Genes

Literature Cited

1. Adams MD, Kelley JM, Gocayne JD, Dubnick M, Polymeropoulos MH. et al. 1991. Complementary DNA sequencing: expressed sequence tags and human genome project. Science 252:1651–56 [Google Scholar]
2. Antonarakis SE, McKusick VA. 2002. OMIM reaches the 1,000-gene mark. Nature 25:1 [Google Scholar]
3. Bannerman RM, Renwick JH. 1962. The hereditary elliptocytoses: clinical and linkage data. Ann. Hum. Genet. 26:23–38 [Google Scholar]
4. Beighton P. ed. 1993. McKusick's Heritable Disorders of Connective Tissue St. Louis: Mosby, 5th ed..
5. Bergsma D, McKusick VA, Dorst JP, Scott CI. eds. 1969. The first conference on the clinical delineation of birth defects. Part IV. Skeletal dysplasias. Birth Defects Orig. Art. Ser. 5:1–396 [Google Scholar]
6. Botstein D, White RL, Skolnick M, Davis RW. 1980. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am. J. Hum. Genet. 32:314–31 [Google Scholar]
7. Bridges CB. 1916. Nondisjunction as proof of the chromosome theory of heredity. Genetics 1:1–52–107–63 [Google Scholar]
8. Bruwer A, Bargen JA, Kierland RR. 1954. Surface pigmentation and generalized intestinal polyposis (Peutz-Jeghers syndrome). Mayo Clin. Proc. 29:168–71 [Google Scholar]
9. Bull LN, van Eijk MJT, Pawlikowska L, DeYoung JA, Juijn JA. et al. 1998. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis. Nat. Genet. 18:21–24 [Google Scholar]
10. Carson NAJ, Cusworth DC, Dent CE, Field CMB, Neill DW, Westall RG. 1963. Homocystinuria: a new inborn error of metabolism associated with mental deficiency. Arch. Dis. Child. 38:425–36 [Google Scholar]
11. Carson NAJ, Neill DW. 1962. Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland. Arch. Dis. Child. 37:505–13 [Google Scholar]
12. Clayton RJ, Iber FL, Ruebner BH, McKusick VA. 1969. Byler disease: fatal familial intrahepatic cholestasis in an Amish kindred. Am. J. Dis. Child. 117:112–24 [Google Scholar]
13. Cross HE, McKusick VA. 1967. The Mast syndrome: a recessively inherited form of presenile dementia with motor disturbances. Arch. Neurol. 16:1–13 [Google Scholar]
14. Cross HE, McKusick VA. 1967. The Troyer syndrome: a recessive form of spastic paraplegia with distal muscle wasting. Arch. Neurol. 16:473–85 [Google Scholar]
15. Cushing H. 1916. Hereditary anchylosis of proximal phalangeal joints (symphalangism). Genetics 1:90–106 [Google Scholar]
16. Donahue RP, Bias WB, Renwick JH, McKusick VA. 1968. Probable assignment of the Duffy blood group locus to chromosome 1 in man. Proc. Natl. Acad. Sci. USA 61:949–55 [Google Scholar]
17. Dulbecco R. 1986. A turning point in cancer research: sequencing the human genome. Science 231:1055–56 [Google Scholar]
18. Ellis NA, Tippett P, Petty A, Reid M, Weller PA. et al. 1994. PBDX is the XG blood group gene. Nat. Genet. 8:285–90 [Google Scholar]
19. Ellis RWB, van Creveld S. 1940. A syndrome characterized by ectodermal dysplasia, polydactyly, chondro-dysplasia and congenital morbus cordis: report of three cases. Arch. Dis. Child. 15:65–84 [Google Scholar]
20. Deleted in proof
21. Evans DAP, Manley KA, McKusick VA. 1960. Genetic control of isoniazid metabolism in man. Br. Med. J. 2:485–91 [Google Scholar]
22. Ferguson-Smith MA, Aitken DA. 1978. Gene dosage: further information on the regional position of the ABO:Np:AK-1 linkage group on chromosome 9. Cytogenet. Cell Genet. 22:449–51 [Google Scholar]
23. Ferguson-Smith MA, Aitken DA, Turleau C, deGrouchy J. 1976. Localisation of the human ABO: Np-1 linkage group by regional assignment of AK-1 to 9q34. Hum. Genet. 34:35–43 [Google Scholar]
24. Fleischmann RD, Adams MD, White O, Clayton RA, Kirkness EF. et al. 1995. Whole-genome random sequencing and assembly of Haemophilus influenzae Rd. Science 269:496–512 [Google Scholar]
25. Francomano CA, Biesecker LG. eds. 2003. Medical genetic studies in the Amish. Am. J. Med. Genet. C 121:1–83 [Google Scholar]
26. Fuller JL, McKusick VA. 1961. A short course in medical genetics. Eugen. Q. 8:98 [Google Scholar]
27. Greenwald R. 2005. …And a diagnostic test was performed. N. Engl. J. Med. 353:2089–90 [Google Scholar]
28. Guethlein LA. 1990. The Bar Harbor Course: a 30-year veteran in the teaching of human genetics. Am. J. Hum. Genet. 46:192–206 [Google Scholar]
29. Haldane JBS. 1948. The formal genetics of man. Proc. R. Soc 135:147–70 [Google Scholar]
30. Haldane JBS, Smith CAB. 1947. A new estimate of the linkage between the genes for color-blindness and hemophilia in man. Ann. Eugen. 14:10–31 [Google Scholar]
31. Hamosh A, Scott AF, Amberger JS, Bocchini CA, McKusick VA. 2005. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res. 33:D514–71 [Google Scholar]
32. Harper PS, Bias WB, Hutchinson JR, McKusick VA. 1971. ABH secretor status of the fetus: a genetic marker identifiable by amniocentesis. J. Med. Genet. 8:438–40 [Google Scholar]
33. Harper PS, Rivas ML, Bias WB, Hutchinson JR, Dyken PR. et al. 1972. Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci. Am. J. Hum. Genet. 24:310–16 [Google Scholar]
34. Heyssel RM, Gaintner JR, Kues IW, Jones AA, Lipstein SH. 1984. Decentralized management in a teaching hospital. N. Engl. J. Med. 310:1477–80 [Google Scholar]
35. Holt M, Oram S. 1960. Familial heart disease with skeletal malformations. Br. Heart J. 22:236–42 [Google Scholar]
36. Hutchinson J. 1896. Pigmentation of lips and mouth. Arch. Surg. 7:290 [Google Scholar]
37. Jeghers H, McKusick VA, Katz KH. 1949. Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits. N. Engl. J. Med. 211:993–1005–1031–36 [Google Scholar]
38. Kucherlapati RS, McKusick VA, Ruddle FH. 1996. Genomics: an established discipline, a commonly used name, a mature journal. Genomics 31:1–2 [Google Scholar]
39. Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC. et al. 2001. Initial sequencing and analysis of the human genome. Nature 49:860–921 Erratum. 2001. Nature 411:720, 412:565 [Google Scholar]
40. Levin LS, Perin JCS, Ose L, Dorst JP, Miller JD, McKusick VA. l977. A heritable syndrome of craniosynostosis, short thin hair, dental abnormalities, and short limbs: cranioectodermal dysplasia. J. Pediat. 90:55–61 [Google Scholar]
41. Lux SEJ, Johnston RB, August CS, Say B, Penschaszadeh VB. et al. 1970. Chronic neutropenia and abnormal cellular immunity in cartilage-hair hypoplasia. N. Engl. J. Med. 282:321–36 [Google Scholar]
42. Makitie O. 1992. Cartilage-hair hypoplasia in Finland: epidemiological and genetic aspects of 107 patients. J. Med. Genet. 29:652–55 [Google Scholar]
43. Makitie O, Kaitila I. 1993. Cartilage-hair hypoplasia—clinical manifestations in 108 Finnish patients. Eur. J. Pediatr 152:211–17 [Google Scholar]
44. Mann JD, Cahan A, Gelb AG, Fisher N, Hamper J. et al. 1962. A sex-linked blood group. Lancet 1:8–10 [Google Scholar]
45. McKusick VA. 1952. The clinical observations of Jonathan Hutchinson. Am. J. Syph. Gonorrhea Vener. Dis 36:101–26 [Google Scholar]
46. McKusick VA. 1952. Chronic constrictive pericarditis. I. Some clinical and laboratory observations. Bull. Johns Hopkins Hosp. 90:3–26 [Google Scholar]
47. McKusick VA. 1952. Chronic constrictive pericarditis. II. Electrokymographic studies and correlations with roentgenkymography, phonocardiography, and right ventricular pressure curves. Bull. Johns Hopkins Hosp. 90:27–41 [Google Scholar]
48. McKusick VA. 1954. The effect of lithium on the electrocardiogram of animals and the relation of this effect to the ratio of the intracellular and extracellular concentrations of potassium. J. Clin. Invest 33:598–610 [Google Scholar]
49. McKusick VA. 1955. The cardiovascular aspects of Marfan's syndrome: a heritable disorder of connective tissue. Circulation 11:321–42 [Google Scholar]
50. McKusick VA. 1956. Heritable Disorders of Connective Tissue St. Louis: Mosby, 1st ed..
51. McKusick VA. 1958. Cardiovascular Sound in Health and Disease Baltimore, MD: Williams & Wilkins570 pp.
52. McKusick VA. 1960. Walter S. Sutton and the physical basis of Mendelism. Bull. Hist. Med. 34:487–97 [Google Scholar]
53. McKusick VA. 1962. On the X chromosome of man. Q. Rev. Biol. 37:69–175 [Google Scholar]
54. McKusick VA. 1963. Frederick Parkes Weber–1863–1962. JAMA 183:45–59 [Google Scholar]
55. McKusick VA. 1964. Human Genetics Englewood Cliffs, NJ: Prentice-Hall148 pp. , 1st ed..
56. McKusick VA. 1964. On the X Chromosome of Man Washington, DC: AIBS
57. McKusick VA. 1966. Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive and X-linked Phenotypes Baltimore, MD: Johns Hopkins Univ. Press, 1st ed..
58. McKusick VA. 1969. Lumpers and splitters, or the nosology of genetic disease. Birth Defects Orig. Art. Ser. 5:23–32 [Google Scholar]
59. McKusick VA. 1969. On lumpers and splitters, or the nosology of genetic disease. Perspect. Biol. Med. 12:298–312 [Google Scholar]
60. McKusick VA. 1970. Prospects for progress. In Congenital Malformations. 3rd Int. Conf., The Hague, 1969 ed. FC Fraser, VA McKusick 3407 Amsterdam: Excerpta Medica [Google Scholar]
61. McKusick VA. 1972. The Bar Harbor course in medical genetics. Science 176:820–21 [Google Scholar]
62. McKusick VA. 1975. A plan for reorganization of the Osler Medical Service. Johns Hopkins Med. J. 136:231–37 [Google Scholar]
63. McKusick VA. 1975. The growth and development of human genetics as a clinical discipline. Am. J. Hum. Genet. 27:261–73 [Google Scholar]
64. McKusick VA. ed. 1978. Medical Genetic Studies of the Amish: Selected Papers Baltimore, MD: Johns Hopkins Univ. Press523 pp. [Google Scholar]
65. McKusick VA. 1978. The William Allan Memorial Award Lecture: Genetic nosology: three approaches. Am. J. Hum. Genet. 30:105–22 [Google Scholar]
66. McKusick VA. 1980. The anatomy of the human genome. Am. J. Med. 60:267–76 [Google Scholar]
67. McKusick VA. 1980. The anatomy of the human genome: the Wilhelmine E. Key 1979 Invitational Lecture. J. Hered. 71:370–91 [Google Scholar]
68. McKusick VA. 1980. The human genome through the eyes of Mercator and Vesalius. Trans. Am. Clin. Climatol. Assoc. 92:66–90 [Google Scholar]
69. McKusick VA. 1985. Marcella O'Grady Boveri (1865–1950) and the chromosome theory of cancer. J. Med. Genet. 22:431–40 [Google Scholar]
70. McKusick VA. 1986. The gene map of Homo sapiens: status and prospectus. Cold Spring Harbor Symp. Quant. Biol. 51:15–27 [Google Scholar]
71. McKusick VA. 1986. The morbid anatomy of the human genome: a review of gene mapping in clinical medicine (four parts). Medicine 65:1–33 1987. 66:1–63. 1988. 66:237–96. 1988. 67:1–19 [Google Scholar]
72. McKusick VA. 1989. HUGO News: The Human Genome Organisation: history, purposes and membership. Genomics 5:385–87 [Google Scholar]
73. McKusick VA. 1993. Medical genetics: a 40-year perspective on the evolution of a medical specialty from a basic science. JAMA 270:2351–56 [Google Scholar]
74. McKusick VA. 1993. Medical Genetics: A Self-Instruction Guide and Workbook Based on Mendelian Inheritance in Man Baltimore, MD: Johns Hopkins Univ. Press126 pp. [Google Scholar]
75. McKusick VA. 1998. Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders Baltimore, MD: Johns Hopkins Univ. Press, 12th ed.. 3 vol.
76. McKusick VA. 1999. Abner McGehee Harvey 1911–1998. Trans. Assoc. Am. Physicians 111:365–68 [Google Scholar]
77. McKusick VA. 2000. A. McGehee Harvey: 30 July 1911–8 May 1998. Proc. Am. Philos. Soc. 144:85–94 [Google Scholar]
78. McKusick VA. 2001. The anatomy of the human genome: a neo-Vesalian basis for medicine in the 21st century. JAMA 286:2289–95 [Google Scholar]
79. McKusick VA. 2002. History of medical genetics. In Emery-Rimoin Principles and Practice of Medical Genetics ed. DL Rimoin, JM Connor, RE Pyeritz, BR Korf pp. 3–36 Edinburgh: Churchill Livingstone., 4th ed.. [Google Scholar]
80. McKusick VA, Amberger JS. 1994. The morbid anatomy of the human genome: chromosomal location of mutations causing disease (update 1 Dec. 1993). J. Med. Genet. 3:265–79 [Google Scholar]
81. McKusick VA and staff. 1961. Medical Genetics 1958–1960. An Annotated Review St. Louis: Mosby
82. McKusick VA and staff. 1964. Medical genetics 1963. J. Chronic Dis 17:1077–1215 [Google Scholar]
83. McKusick VA and staff. 1965. Medical Genetics 1961–1963. An Annotated Review Oxford: Pergamon
84. McKusick VA, Bauer RL, Koop CE, Scott RB. 1964. Hydrometrocolpos as a simply inherited malformation. JAMA 189:813–16 [Google Scholar]
85. McKusick VA, Egeland JA, Eldridge R, Krusen DE. 1964. Dwarfism in the Amish. I. The Ellis-van Creveld syndrome. Bull. Johns Hopkins Hosp. 115:307–36 [Google Scholar]
86. McKusick VA, Eldridge R, Hostetler JA, Ruangwit U, Egeland JA. 1964. Dwarfism in the Amish. II. Cartilage-hair hypoplasia. Bull. Johns Hopkins Hosp. 116:285–326 [Google Scholar]
87. McKusick VA, Harris WS, Ottesen OE, Goodman RM, Sheeley WM, Bloodwell RO. 1962. Buerger's disease: a distinct clinical and pathologic entity. JAMA 181:5–l2 [Google Scholar]
88. McKusick VA, Hostetler JA, Egeland JA. 1964. Genetic studies of the Amish: background and potentialities. Bull. Johns Hopkins Hosp. 115:203–22 [Google Scholar]
89. McKusick VA, Hostetler JA, Egeland JA, Eldridge R. 1964. The distribution of certain genes in the Old Order Amish. Cold Spring Harbor Symp. Quant. Biol. 29:99–113 [Google Scholar]
90. McKusick VA, Howell RR, Hussels IE, Neufeld F, Stevenson RE. 1972. Allelism, nonallelism and genetic compounds among the mucopolysaccharidoses. Lancet 1:993–96 [Google Scholar]
91. McKusick VA, Kaplan D, Wise D, Hanley WB, Suddarth SB. et al. 1965. The genetic mucopolysaccharidoses. Medicine 44:445–83 [Google Scholar]
92. McKusick VA, Naggert J, Nishina P, Valle D. 1999. Forty years of the annual ‘Bar Harbor Course’ (1960–1999): a pictorial history. Clin. Genet. 55:398–415 [Google Scholar]
93. McKusick VA, Ruddle FH. 1977. The status of the gene map of the human chromosomes. Science 196:390–405 [Google Scholar]
94. McKusick VA, Ruddle FH. 1987. A new discipline, a new name, a new journal. Genomics 1:1–2 [Google Scholar]
95. McKusick VA, Stauffer M, Knox DL, Clark DB. 1966. Chorioretinopathy with hereditary microcephaly. Arch. Ophthalmol 75:587–600 [Google Scholar]
96. McKusick VA, Talbot SA, Webb GN. 1954. Spectral phonocardiography: problems and prospects in the application of the Bell sound spectrograph to phonocardiography. Bull. Johns Hopkins Hosp. 94:187–98 [Google Scholar]
97. McKusick VA, Webb GN, Bradshaw JR, Talbot SA. 1954. Spectral phonocardiography: clinical studies. Bull. John Hopkins Hosp. 95:90–110 [Google Scholar]
98. McKusick VA, Wiskind HK. 1959. Osborne Reynolds of Manchester: contributions of an engineer to the understanding of cardiovascular sound. Bull. Hist. Med. 33:116–35 [Google Scholar]
99. Migeon BR, Miller CS. 1968. Human-mouse somatic cell hybrids with single human chromosome (group E): link with thymidine kinase activity. Science 162:1005–6 [Google Scholar]
100. Mohr J. 1951. Estimation of linkage between the Lutheran and the Lewis blood groups. Acta Pathol. Microbiol. Scand 29:339–44 [Google Scholar]
101. Morton NE. 1956. The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type. Am. J. Hum. Genet. 8:80–96 [Google Scholar]
102. Motulsky AG. 1957. Drug reactions, enzymes, and biochemical genetics. JAMA 165:835–37 [Google Scholar]
103. NRC/NAS Comm. Mapp. Sequen. Hum. Genome. 1988. Mapping and Sequencing the Human Genome Washington, DC: Natl. Acad. Press
104. Online Mendelian Inheritance in Man, OMIM (TM). McKusick-Nathans Inst. Genet. Med. Johns Hopkins Univ. (Baltimore, MD) and Natl. Cent. Biotechnol. Info., Natl. Libr. Med. (Bethesda, MD) 2006. http://www.ncbi.nlm.nih.gov/omim/
105. Patel H, Cross H, Proukakis C, Hershberger R, Bork P. et al. 2002. SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia. Nat. Genet. 31:347–48 [Google Scholar]
106. Peutz JLA. 1921. Very remarkable case of familial polyposis of mucous membrane of intestinal tract and nasopharynx accompanied by peculiar pigmentations of skin and mucous membrane. (Dutch). Ned. Maandschr. Geneeskd 10:134–46 [Google Scholar]
107. Porter IH, Schulze J, McKusick VA. 1962. Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and color-blindness in American Negroes. Ann. Hum. Genet. 26:107–22 [Google Scholar]
108. Porter IH, Schulze J, McKusick VA. 1962. Linkage between glucose 6-phosphate dehydrogenase and color-blindness. Nature 193:506 [Google Scholar]
109. Renwick JH. 1971. The mapping of human chromosomes. Annu. Rev. Genet 5:81–120 [Google Scholar]
110. Renwick JH, Bolling D. 1967. A program-complex for encoding, analyzing, and storing human linkage data. Am. J. Hum. Genet. 19:360–67 [Google Scholar]
111. Renwick JH, Lawler SD. 1955. Genetical linkage between the ABO and nail-patella loci. Ann. Hum. Genet. 19:312–31 [Google Scholar]
112. Renwick JH, Schulze J. 1961. A computer program for the processing of linkage data from large pedigrees. Excerpta Med. Int. Congr. Ser. 32E145 2nd Int. Conf. Hum. Genet., Rome (Abstr.):
113. Renwick JH, Schulze J. 1964. An analysis of some data on the linkage between XG and colorblindness in man. Am. J. Hum. Genet. 16:410–18 [Google Scholar]
114. Deleted in proof
115. Ridanpaa M, Jain P, McKusick VA, Francomano CA, Kaitila I. 2003. The major mutation in the RMRP gene causing CHH among the Amish is the same as that found in most Finnish cases. Am. J. Med. Genet. C 121:81–83 [Google Scholar]
116. Rimoin DL, Merimee TJ, McKusick VA. 1965. Growth hormone deficiency in man: an isolated, recessively inherited defect. Science 182:1635 [Google Scholar]
117. Ruddle FH, Chapman VM, Chen T-R, Klebe RJ. 1970. Linkage between human lactate dehydrogenase A and B and peptidase B. Nature 227:251–57 [Google Scholar]
118. Santachiara AS, Nabholz M, Miggiano V, Darlington AJ, Bodmer W. 1970. Genetic analysis with man-mouse somatic cell hybrids. Linkage between human lactate dehydrogenase B and peptidase B genes. Nature 227:248–51 [Google Scholar]
119. Saulsbury FT, Winkelstein JA, Davis LE, Hsu S, Souza B. et al. 1975. Combined immunodeficiency and vaccine-related poliomyelitis in a child with cartiliage-hair hypoplasia. J. Pediatr. 86:868–72 [Google Scholar]
120. Schimke RN, McKusick VA, Huang T, Pollack AD. 1965. Homocystinuria: studies of 20 families with 38 affected members. JAMA 193:711–19 [Google Scholar]
121. Schleutermann CA, Bias WB, Murdoch JL, McKusick VA. 1969. Linkage of the loci for the nail-patella syndrome and adenylate kinase. Am. J. Hum. Genet. 21:606–30 [Google Scholar]
122. Schleutermann CA, Murdoch JL, Walker BA, Bias WB, Chase GA. et al. 1976. A linkage study of the Marfan syndrome. Clin. Genet. 10:51–53 [Google Scholar]
123. Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R. et al. 2003. Maspardin is mutated in Mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia. Am. J. Hum. Genet. 73:1147–56 [Google Scholar]
124. Southworth JL, McKusick VA, Pierce EC II, Rawson FLJ. 1950. Ventricular fibrillation precipitated by cardiac catheterization: complete recovery of the patient after 45 minutes. JAMA 143:717–20 [Google Scholar]
125. Stern C. 1949. Principles of Human Genetics San Francisco: Freeman, lst ed..
126. Stone DL, Slavotinek A, Bouffard GG, Banerjee-Basu S, Baxevanis AD. et al. 2000. Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome. Nat. Genet. 25:79–82 [Google Scholar]
127. Strasburger AK, Hawkins MR, Eldridge R, Hargrave RL, McKusick VA. 1965. Symphalangism: genetic and clinical aspects. Bull. Johns Hopkins Hosp. 117:108–27 [Google Scholar]
128. Sulston J, Ferry G. 2002. The Common Thread: A Story of Science, Politics, Ethics, and the Human Genome Washington, DC: Natl. Acad. Press, 1st ed.. [Google Scholar]
129. Temtamy SA, McKusick VA. 1978. The Genetics of Hand Malformations New York: Alan R. Liss, Inc.
130. Venter JC, Adams MD, Myers EW, Li PW, Mural RJ. et al. 2001. The sequence of the human genome. Science 291:1304–51 Erratum. 2001. Science 292:1838 [Google Scholar]
131. Vogel F. 1959. Moderne Probleme der Humangenetik. Ergeb. Inn. Med. Kinderheilkd 12:52–125 [Google Scholar]
132. Weber FP. 1919. Patches of deep pigmentation of oral mucous membrane not connected with Addison's disease. Q. J. Med. 12:404 [Google Scholar]
133. Weiss MC, Green H. 1967. Human-mouse hybrid cell lines containing partial complements of human chromosomes and functioning human genes. Proc. Natl. Acad. Sci. USA 58:1104–11 [Google Scholar]
134. Ying KL, Ives EJ. 1968. Asymmentry of chromosome number 1 pair in three generations of a phenotypically normal family. Canadian J. Genet. Cytol. 10:575–89 [Google Scholar]