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I Winship

Showing results (1-10 of 37) with videos related to

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South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 7, 1986
Epidermolysis bullosa in South AfricaI Winship
Clinical Dysmorphology|May 13, 1999
A patient with VACTERL association, amelia and hemifacial microsomiaS Aftimos, I Winship
Clinical Dysmorphology|July 1, 1993
Radial ray defect and Robin sequence: a new syndrome?A Bruce, I Winship
Clinical Genetics|April 1, 1992
Phenotypic discriminants in the Waardenburg syndromeI Winship, P Beighton
American Journal of Medical Genetics|December 1, 1984
X-linked inheritance of ocular albinism with late-onset sensorineural deafnessI Winship, G Gericke, P Beighton
Clinical Genetics|February 28, 2004
Autosomal dominant velopharyngeal insufficiency: father-to-son transmission confirmedP Kannu, S Aftimos, I Winship
Internal Medicine Journal|October 11, 2014
Author reply: To PMID 24750312M Salaria, P Mitchell, I Winship
Clinical Genetics|July 1, 1985
The ocular form of osteogenesis imperfecta: a new autosomal recessive syndromeP Beighton, I Winship, D Behari
American Journal of Medical Genetics|August 1, 1990
Boomerang dysplasiaI Winship, B Cremin, P Beighton
Clinical Dysmorphology|October 23, 2001
Clinical phenotypes of nine cases of Kabuki syndrome from New ZealandJ McGaughran, S Aftimos, C Jefferies, et al.
Pageof 4

Showing results (1-10 of 37) with videos related to

Sort By:
Pageof 4
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|June 7, 1986
Epidermolysis bullosa in South AfricaI Winship
Clinical Dysmorphology|May 13, 1999
A patient with VACTERL association, amelia and hemifacial microsomiaS Aftimos, I Winship
Clinical Dysmorphology|July 1, 1993
Radial ray defect and Robin sequence: a new syndrome?A Bruce, I Winship
Clinical Genetics|April 1, 1992
Phenotypic discriminants in the Waardenburg syndromeI Winship, P Beighton
American Journal of Medical Genetics|December 1, 1984
X-linked inheritance of ocular albinism with late-onset sensorineural deafnessI Winship, G Gericke, P Beighton
Clinical Genetics|February 28, 2004
Autosomal dominant velopharyngeal insufficiency: father-to-son transmission confirmedP Kannu, S Aftimos, I Winship
Internal Medicine Journal|October 11, 2014
Author reply: To PMID 24750312M Salaria, P Mitchell, I Winship
Clinical Genetics|July 1, 1985
The ocular form of osteogenesis imperfecta: a new autosomal recessive syndromeP Beighton, I Winship, D Behari
American Journal of Medical Genetics|August 1, 1990
Boomerang dysplasiaI Winship, B Cremin, P Beighton
Clinical Dysmorphology|October 23, 2001
Clinical phenotypes of nine cases of Kabuki syndrome from New ZealandJ McGaughran, S Aftimos, C Jefferies, et al.
Pageof 4