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Journal of Medical Genetics
|
August 1, 1990
The Moebius syndrome: aetiology, incidence of mental retardation, and genetics
T Lipson, W Webster, D D Weaver
Clinical Dysmorphology
|
July 1, 1996
Oculo-auriculo-vertebral spectrum and the CHARGE association: clinical evidence for a common pathogenetic mechanism
T D Van Meter, D D Weaver
Clinical Genetics
|
March 1, 1978
Phenotypic and genetic analysis of the silver-Russell syndrome
V Escobar, S Gleiser, D D Weaver
American Journal of Human Genetics
|
May 1, 1993
Concerns about the genetics of pre-eclampsia
T D Van Meter, D D Weaver
Journal of Medical Genetics
|
June 4, 1998
49,XXXXY: a distinct phenotype. Three new cases and review
J Peet, D D Weaver, G H Vance
American Journal of Medical Genetics
|
January 10, 1997
Molecular cytogenetic identification of four X chromosome duplications
A Zhang, D D Weaver, C G Palmer
American Journal of Diseases of Children (1960)
|
April 1, 1986
Analysis of growth in the VATER association
C L Mapstone, D D Weaver, P L Yu
Pediatric Neurology
|
September 1, 1993
Benign hereditary chorea
P G Wheeler, D D Weaver, W B Dobyns
American Journal of Medical Genetics
|
February 27, 2001
Distal 13q Deletion Syndrome and the VACTERL association: case report, literature review, and possible implications
L E Walsh, G H Vance, D D Weaver
American Journal of Medical Genetics
|
February 13, 1995
Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome
P G Wheeler, D D Weaver, C G Palmer
Page
of 10
Search research articles
Search
Showing results (21-30 of 99) with videos related to
Sort By:
Page
of 10
Journal of Medical Genetics
|
August 1, 1990
The Moebius syndrome: aetiology, incidence of mental retardation, and genetics
T Lipson, W Webster, D D Weaver
Clinical Dysmorphology
|
July 1, 1996
Oculo-auriculo-vertebral spectrum and the CHARGE association: clinical evidence for a common pathogenetic mechanism
T D Van Meter, D D Weaver
Clinical Genetics
|
March 1, 1978
Phenotypic and genetic analysis of the silver-Russell syndrome
V Escobar, S Gleiser, D D Weaver
American Journal of Human Genetics
|
May 1, 1993
Concerns about the genetics of pre-eclampsia
T D Van Meter, D D Weaver
Journal of Medical Genetics
|
June 4, 1998
49,XXXXY: a distinct phenotype. Three new cases and review
J Peet, D D Weaver, G H Vance
American Journal of Medical Genetics
|
January 10, 1997
Molecular cytogenetic identification of four X chromosome duplications
A Zhang, D D Weaver, C G Palmer
American Journal of Diseases of Children (1960)
|
April 1, 1986
Analysis of growth in the VATER association
C L Mapstone, D D Weaver, P L Yu
Pediatric Neurology
|
September 1, 1993
Benign hereditary chorea
P G Wheeler, D D Weaver, W B Dobyns
American Journal of Medical Genetics
|
February 27, 2001
Distal 13q Deletion Syndrome and the VACTERL association: case report, literature review, and possible implications
L E Walsh, G H Vance, D D Weaver
American Journal of Medical Genetics
|
February 13, 1995
Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome
P G Wheeler, D D Weaver, C G Palmer
Page
of 10