Gericke GS - Search Results

1

Acrocallosal syndrome in two African brothers born to consanguineous parents.

Christianson AL, Venter PA, Du Toit JL, Shipalana N, Gericke GS. Christianson AL, et al. Among authors: gericke gs. Am J Med Genet. 1994 Jun 1;51(2):98-101. doi: 10.1002/ajmg.1320510204. Am J Med Genet. 1994. PMID: 8092201

2

Congenital anomalies in black South African liveborn neonates at an urban academic hospital.

Delport SD, Christianson AL, van den Berg HJ, Wolmarans L, Gericke GS. Delport SD, et al. Among authors: gericke gs. S Afr Med J. 1995 Jan;85(1):11-5. S Afr Med J. 1995. PMID: 7784907

3

Congenital anomalies in rural black South African neonates--a silent epidemic?

Venter PA, Christianson AL, Hutamo CM, Makhura MP, Gericke GS. Venter PA, et al. Among authors: gericke gs. S Afr Med J. 1995 Jan;85(1):15-20. S Afr Med J. 1995. PMID: 7784908

4

Genetics, primary health care and the Third World.

Christianson AL, Gericke GS, Venter PA, du Toit JL. Christianson AL, et al. Among authors: gericke gs. S Afr Med J. 1995 Jan;85(1):6-7. S Afr Med J. 1995. PMID: 7784935 No abstract available.

5

Chromosome markers and mental retardation.

Venter PA, Gericke GS. Venter PA, et al. Among authors: gericke gs. S Afr Med J. 1981 Feb 7;59(6):170. S Afr Med J. 1981. PMID: 6936840 No abstract available.

6

A marker X chromosome associated with nonspecific male mental retardation. The first South African cases.

Venter PA, Gericke GS, Dawson B, Op't Hof J. Venter PA, et al. Among authors: gericke gs. S Afr Med J. 1981 Nov 21;60(21):807-11. S Afr Med J. 1981. PMID: 7302747

7

Marker X chromosomes in nonspecific male mental retardation.

Venter PA, Gericke GS. Venter PA, et al. Among authors: gericke gs. S Afr Med J. 1980 Jun 28;57(26):1066. S Afr Med J. 1980. PMID: 7190736 No abstract available.

8

Increased chromosomal breakage in Tourette syndrome predicts the possibility of variable multiple gene involvement in spectrum phenotypes: preliminary findings and hypothesis.

Gericke GS, Simonic I, Cloete E, Buckle C, Becker PJ. Gericke GS, et al. Am J Med Genet. 1995 Oct 9;60(5):444-7. doi: 10.1002/ajmg.1320600516. Am J Med Genet. 1995. PMID: 8546159

9

Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners.

Simonic I, Nyholt DR, Gericke GS, Gordon D, Matsumoto N, Ledbetter DH, Ott J, Weber JL. Simonic I, et al. Among authors: gericke gs. Am J Med Genet. 2001 Mar 8;105(2):163-7. doi: 10.1002/ajmg.1192. Am J Med Genet. 2001. PMID: 11304830

10

Additional clinical and cytogenetic findings associated with Rett syndrome.

Simonic I, Gericke GS, Lippert M, Schoeman JF. Simonic I, et al. Among authors: gericke gs. Am J Med Genet. 1997 May 31;74(3):331-7. Am J Med Genet. 1997. PMID: 9184319

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