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South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
June 7, 1986
Epidermolysis bullosa in South Africa
I Winship
Clinical Dysmorphology
|
May 13, 1999
A patient with VACTERL association, amelia and hemifacial microsomia
S 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 syndrome
I Winship, P Beighton
American Journal of Medical Genetics
|
December 1, 1984
X-linked inheritance of ocular albinism with late-onset sensorineural deafness
I Winship, G Gericke, P Beighton
Clinical Genetics
|
February 28, 2004
Autosomal dominant velopharyngeal insufficiency: father-to-son transmission confirmed
P Kannu, S Aftimos, I Winship
Internal Medicine Journal
|
October 11, 2014
Author reply: To PMID 24750312
M Salaria, P Mitchell, I Winship
Clinical Genetics
|
July 1, 1985
The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome
P Beighton, I Winship, D Behari
American Journal of Medical Genetics
|
August 1, 1990
Boomerang dysplasia
I Winship, B Cremin, P Beighton
Clinical Dysmorphology
|
October 23, 2001
Clinical phenotypes of nine cases of Kabuki syndrome from New Zealand
J McGaughran, S Aftimos, C Jefferies, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 37) with videos related to
Sort By:
Page
of 4
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
June 7, 1986
Epidermolysis bullosa in South Africa
I Winship
Clinical Dysmorphology
|
May 13, 1999
A patient with VACTERL association, amelia and hemifacial microsomia
S 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 syndrome
I Winship, P Beighton
American Journal of Medical Genetics
|
December 1, 1984
X-linked inheritance of ocular albinism with late-onset sensorineural deafness
I Winship, G Gericke, P Beighton
Clinical Genetics
|
February 28, 2004
Autosomal dominant velopharyngeal insufficiency: father-to-son transmission confirmed
P Kannu, S Aftimos, I Winship
Internal Medicine Journal
|
October 11, 2014
Author reply: To PMID 24750312
M Salaria, P Mitchell, I Winship
Clinical Genetics
|
July 1, 1985
The ocular form of osteogenesis imperfecta: a new autosomal recessive syndrome
P Beighton, I Winship, D Behari
American Journal of Medical Genetics
|
August 1, 1990
Boomerang dysplasia
I Winship, B Cremin, P Beighton
Clinical Dysmorphology
|
October 23, 2001
Clinical phenotypes of nine cases of Kabuki syndrome from New Zealand
J McGaughran, S Aftimos, C Jefferies, et al.
Page
of 4