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American Journal of Medical Genetics|October 1, 1992
Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5L D Keppen, S M Gollin, D Edwards, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 7, 1975
Clinical and cytogenetic aspects of the 21 deletion syndromeG S Gericke, M F Steyn, A E Retief, et al.
Journal of Medical Genetics|April 1, 1989
Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locusM J Kotze, E Langenhoven, A E Retief, et al.
American Journal of Human Genetics|June 1, 1995
Evidence for a distinct region causing a cat-like cry in patients with 5p deletionsM Gersh, S A Goodart, L M Pasztor, et al.
Arthritis and Rheumatism|October 19, 1999
Exclusion of the gene for human cartilage intermediate layer protein in currently mapped calcium pyrophosphate dihydrate deposition syndromesR C Marinescu, K Nyce, L Serrano de la Peña, et al.
Cancer Research|November 21, 1998
Refined chromosomal localization of the mismatch repair and hereditary nonpolyposis colorectal cancer genes hMSH2 and hMSH6C Schmutte, R C Marinescu, N G Copeland, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|January 8, 1983
A 3-year cytogenetic survey of 9 661 patients in South AfricaA E Retief, R Bernstein, H J Grace, et al.
International Journal of Fertility|January 1, 1975
Oligozoospermia: a seven-year survey of the incidence, chromosomal aberrations, treatment and pregnancy rateJ A van Zyl, R Menkveld, T J van Kotze, et al.
Human Genetics|December 1, 1993
The human cytochrome b5 gene and two of its pseudogenes are located on chromosomes 18q23, 14q31-32.1 and 20p11.2, respectivelyS J Giordano, M Yoo, D C Ward, et al.
American Journal of Human Genetics|November 1, 1995
Physical mapping of the holoprosencephaly critical region in 18p11.3J Overhauser, H F Mitchell, E H Zackai, et al.
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