McKusick VA - Search Results

1

An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.

Borgaonkar DS, McKusick VA, Farber PA. Borgaonkar DS, et al. Among authors: mckusick va. J Med Genet. 1973 Dec;10(4):379-84. doi: 10.1136/jmg.10.4.379. J Med Genet. 1973. PMID: 4129973 Free PMC article.

2

Chromosomal variation in man: catalog of chromosomal variants and anomalies.

Borgaonkar DS, Bolling DR, Partridge C, Ruddle FH, McKusick VA. Borgaonkar DS, et al. Among authors: mckusick va. Cytogenet Cell Genet. 1975;14(3-6):252-4. doi: 10.1159/000130355. Cytogenet Cell Genet. 1975. PMID: 1192796 No abstract available.

3

Constancy of the length of human Y chromosome.

Borgaonkar DS, McKusick VA, Herr HM, de los Cobos L, Yoder OC. Borgaonkar DS, et al. Among authors: mckusick va. Ann Genet. 1969 Dec;12(4):262-4. Ann Genet. 1969. PMID: 5309419 No abstract available.

4

The YY syndrome.

Borgaonkar DS, Murdoch JL, McKusick VA, Borkowf SP, Money JW, Robinson BW. Borgaonkar DS, et al. Among authors: mckusick va. Lancet. 1968 Aug 24;2(7565):461-2. doi: 10.1016/s0140-6736(68)90509-6. Lancet. 1968. PMID: 4174191 No abstract available.

5

Chromosomal variation in man: catalog of chromosomal variants and anomalies.

Borgaonkar DS, Bolling DR, Partridge C, Ruddle FH, McKusick VA. Borgaonkar DS, et al. Among authors: mckusick va. Birth Defects Orig Artic Ser. 1975;11(3):82-4. Birth Defects Orig Artic Ser. 1975. PMID: 1203509 No abstract available.

6

Conductive hearing loss and malformed low-set ears, as a possible recessive syndrome.

Mengel MC, Konigsmark BW, Berlin CI, McKusick VA. Mengel MC, et al. Among authors: mckusick va. J Med Genet. 1969 Mar;6(1):14-21. doi: 10.1136/jmg.6.1.14. J Med Genet. 1969. PMID: 5771216 Free PMC article. No abstract available.

7

Marcella O'Grady Boveri (1865-1950) and the chromosome theory of cancer.

McKusick VA. McKusick VA. J Med Genet. 1985 Dec;22(6):431-40. doi: 10.1136/jmg.22.6.431. J Med Genet. 1985. PMID: 3908684 Free PMC article.

8

The morbid anatomy of the human genome: chromosomal location of mutations causing disease.

McKusick VA, Amberger JS. McKusick VA, et al. J Med Genet. 1993 Jan;30(1):1-26. doi: 10.1136/jmg.30.1.1. J Med Genet. 1993. PMID: 8423603 Free PMC article. Review.

9

A gene map of congenital malformations.

Wilkie AO, Amberger JS, McKusick VA. Wilkie AO, et al. Among authors: mckusick va. J Med Genet. 1994 Jul;31(7):507-17. doi: 10.1136/jmg.31.7.507. J Med Genet. 1994. PMID: 7966186 Free PMC article. Review.

10

Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.

Rosenfeld PJ, McKusick VA, Amberger JS, Dryja TP. Rosenfeld PJ, et al. Among authors: mckusick va. J Med Genet. 1994 Dec;31(12):903-15. doi: 10.1136/jmg.31.12.903. J Med Genet. 1994. PMID: 7891370 Free PMC article. Review. No abstract available.

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