Winship WS - Search Results

1

Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.

Southgate L, Machado RD, Snape KM, Primeau M, Dafou D, Ruddy DM, Branney PA, Fisher M, Lee GJ, Simpson MA, He Y, Bradshaw TY, Blaumeiser B, Winship WS, Reardon W, Maher ER, FitzPatrick DR, Wuyts W, Zenker M, Lamarche-Vane N, Trembath RC. Southgate L, et al. Among authors: winship ws. Am J Hum Genet. 2011 May 13;88(5):574-85. doi: 10.1016/j.ajhg.2011.04.013. Am J Hum Genet. 2011. PMID: 21565291 Free PMC article.

2

Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorder.

Kinning E, Tufarelli C, Winship WS, Aldred MA, Trembath RC. Kinning E, et al. Among authors: winship ws. J Med Genet. 2005 Dec;42(12):e70. doi: 10.1136/jmg.2005.033829. J Med Genet. 2005. PMID: 16326827 Free PMC article.

3

The Dyggve-Melchior-Clausen syndrome in Indian siblings.

Winship WS, Rubin DL. Winship WS, et al. Clin Genet. 1992 Nov;42(5):240-5. doi: 10.1111/j.1399-0004.1992.tb03248.x. Clin Genet. 1992. PMID: 1486701

4

Dyssegmental dysplasia in a South African neonate.

Winship WS, Beighton P. Winship WS, et al. Clin Dysmorphol. 2008 Apr;17(2):95-98. doi: 10.1097/MCD.0b013e3282f25136. Clin Dysmorphol. 2008. PMID: 18388778

5

A new form of hypohidrotic ectodermal dysplasia.

Viljoen DL, Winship WS. Viljoen DL, et al. Among authors: winship ws. Am J Med Genet. 1988 Sep;31(1):25-32. doi: 10.1002/ajmg.1320310106. Am J Med Genet. 1988. PMID: 3066219 Review.

6

Pigmentary abnormalities in trisomy of chromosome 13.

Pillay T, Winship WS, Ramdial PK. Pillay T, et al. Among authors: winship ws. Clin Dysmorphol. 1998 Jul;7(3):191-4. doi: 10.1097/00019605-199807000-00006. Clin Dysmorphol. 1998. PMID: 9689992

7

Prader-Willi syndrome in South African patients--clinical and molecular diagnosis.

Christianson AL, Viljoen DL, Winship WS, de la Rey M, van Rensburg EJ. Christianson AL, et al. Among authors: winship ws. S Afr Med J. 1998 Jun;88(6):711-4. S Afr Med J. 1998. PMID: 9687849

8

Genetic disorders in the Indian community of South Africa.

Winship WS, Beighton P. Winship WS, et al. S Afr Med J. 2011 Jun 27;101(7):481-4. S Afr Med J. 2011. PMID: 21920103

9

Epidermolysis bullosa misdiagnosed as child abuse. A report of 3 cases.

Winship IM, Winship WS. Winship IM, et al. Among authors: winship ws. S Afr Med J. 1988 Mar 19;73(6):369-70. S Afr Med J. 1988. PMID: 3353812

10

Congenital heart disease in the South African Bantu: a report of 117 cases.

Van der Horst RL, Winship WS, Pittaway D, Gibb BH, Lapinsky GB. Van der Horst RL, et al. Among authors: winship ws. S Afr Med J. 1968 Dec 7;42(46):1271-3. S Afr Med J. 1968. PMID: 5720136 No abstract available.

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