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European Journal of Pediatrics
|
October 1, 1976
Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases
A L Kosseff, J Herrmann, E F Gilbert, et al.
Birth Defects Original Article Series
|
January 1, 1987
The short umbilical cord
D K Grange, S Arya, J M Opitz, et al.
American Journal of Medical Genetics
|
May 1, 1994
Smith-Lemli-Opitz (RSH) syndrome bibliography: 1964-1993
J M Opitz, V B Penchaszadeh, M C Holt, et al.
Human Heredity
|
January 1, 1973
The Poland syndrome-clinical and genealogical data, dermatoglyphic analysis, and incidence
N Freire-Maia, E A Chautard, J M Opitz, et al.
American Journal of Medical Genetics
|
August 22, 1997
Familial broad terminal phalanges with one individual showing additional anomalies
L Pavone, G Sorge, V Pavone, et al.
The New England Journal of Medicine
|
November 28, 1985
Perinatal mortality due to interaction of diphenhydramine and temazepam
G A Kargas, S A Kargas, H J Bruyere, et al.
American Journal of Medical Genetics
|
March 13, 1995
Asplenia in two father-son pairs
N M Lindor, W A Smithson, C A Ahumada, et al.
Fetal and Pediatric Pathology
|
June 7, 2006
"Double-muscle" trait in cattle: a possible model for Wiedemann-Beckwith syndrome
L G Best, E Gilbert-Barness, D E Gerrard, et al.
American Journal of Medical Genetics
|
January 1, 1980
Virilism as a late manifestation in the Bardet-Biedl syndrome
R V Haning, I H Carlson, E F Gilbert, et al.
American Journal of Medical Genetics
|
December 1, 1985
An autosomal dominant syndrome of short stature with mesomelic shortness of limbs, abnormal carpal and tarsal bones, hypoplastic middle phalanges, and bipartite calcanei
W R Osebold, D J Remondini, E L Lester, et al.
Page
of 34
Search research articles
Search
Showing results (261-270 of 338) with videos related to
Sort By:
Page
of 34
European Journal of Pediatrics
|
October 1, 1976
Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases
A L Kosseff, J Herrmann, E F Gilbert, et al.
Birth Defects Original Article Series
|
January 1, 1987
The short umbilical cord
D K Grange, S Arya, J M Opitz, et al.
American Journal of Medical Genetics
|
May 1, 1994
Smith-Lemli-Opitz (RSH) syndrome bibliography: 1964-1993
J M Opitz, V B Penchaszadeh, M C Holt, et al.
Human Heredity
|
January 1, 1973
The Poland syndrome-clinical and genealogical data, dermatoglyphic analysis, and incidence
N Freire-Maia, E A Chautard, J M Opitz, et al.
American Journal of Medical Genetics
|
August 22, 1997
Familial broad terminal phalanges with one individual showing additional anomalies
L Pavone, G Sorge, V Pavone, et al.
The New England Journal of Medicine
|
November 28, 1985
Perinatal mortality due to interaction of diphenhydramine and temazepam
G A Kargas, S A Kargas, H J Bruyere, et al.
American Journal of Medical Genetics
|
March 13, 1995
Asplenia in two father-son pairs
N M Lindor, W A Smithson, C A Ahumada, et al.
Fetal and Pediatric Pathology
|
June 7, 2006
"Double-muscle" trait in cattle: a possible model for Wiedemann-Beckwith syndrome
L G Best, E Gilbert-Barness, D E Gerrard, et al.
American Journal of Medical Genetics
|
January 1, 1980
Virilism as a late manifestation in the Bardet-Biedl syndrome
R V Haning, I H Carlson, E F Gilbert, et al.
American Journal of Medical Genetics
|
December 1, 1985
An autosomal dominant syndrome of short stature with mesomelic shortness of limbs, abnormal carpal and tarsal bones, hypoplastic middle phalanges, and bipartite calcanei
W R Osebold, D J Remondini, E L Lester, et al.
Page
of 34