Search research articles
Contact Us
Filters
Showing results (41-50 of 99) with videos related to
Page
of 10
Sort By:
The Journal of Pediatrics
|
March 1, 1990
Fetal brain disruption sequence
C A Moore, D D Weaver, M J Bull
Journal of Medical Genetics
|
September 1, 1974
The tricho-rhino-phalangeal syndrome
D D Weaver, M M Cohen, D W Smith
American Journal of Diseases of Children (1960)
|
March 1, 1986
The VATER association. Analysis of 46 patients
D D Weaver, C L Mapstone, P L Yu
Clinical Genetics
|
June 1, 1985
Congenital contractural arachnodactyly. Report of four additional families and review of literature
M A Ramos Arroyo, D D Weaver, R K Beals
American Journal of Medical Genetics
|
June 22, 1999
Bone mineral density and laboratory evaluation of a type II autosomal dominant osteopetrosis carrier
I Takacs, H Cooper, D D Weaver, et al.
American Journal of Medical Genetics
|
February 15, 1993
Otopalatodigital syndrome type II associated with omphalocele: report of three cases
K Young, C K Barth, C Moore, et al.
Human Genetics
|
January 1, 1983
Dicentric chromosome 13 and centromere inactivation
S Schwartz, C G Palmer, D D Weaver, et al.
Pediatrics
|
December 1, 1991
Weaver syndrome: a case without early overgrowth and review of the literature
M A Ramos-Arroyo, D D Weaver, E R Banks
American Journal of Diseases of Children (1960)
|
June 1, 1982
Hyperexplexia: not hereditary stiff-baby syndrome
D D Weaver, D J Morley, B P Garg, et al.
American Journal of Medical Genetics
|
February 1, 1984
In utero brain destruction resulting in collapse of the fetal skull, microcephaly, scalp rugae, and neurologic impairment: the fetal brain disruption sequence
L J Russell, D D Weaver, M J Bull, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 99) with videos related to
Sort By:
Page
of 10
The Journal of Pediatrics
|
March 1, 1990
Fetal brain disruption sequence
C A Moore, D D Weaver, M J Bull
Journal of Medical Genetics
|
September 1, 1974
The tricho-rhino-phalangeal syndrome
D D Weaver, M M Cohen, D W Smith
American Journal of Diseases of Children (1960)
|
March 1, 1986
The VATER association. Analysis of 46 patients
D D Weaver, C L Mapstone, P L Yu
Clinical Genetics
|
June 1, 1985
Congenital contractural arachnodactyly. Report of four additional families and review of literature
M A Ramos Arroyo, D D Weaver, R K Beals
American Journal of Medical Genetics
|
June 22, 1999
Bone mineral density and laboratory evaluation of a type II autosomal dominant osteopetrosis carrier
I Takacs, H Cooper, D D Weaver, et al.
American Journal of Medical Genetics
|
February 15, 1993
Otopalatodigital syndrome type II associated with omphalocele: report of three cases
K Young, C K Barth, C Moore, et al.
Human Genetics
|
January 1, 1983
Dicentric chromosome 13 and centromere inactivation
S Schwartz, C G Palmer, D D Weaver, et al.
Pediatrics
|
December 1, 1991
Weaver syndrome: a case without early overgrowth and review of the literature
M A Ramos-Arroyo, D D Weaver, E R Banks
American Journal of Diseases of Children (1960)
|
June 1, 1982
Hyperexplexia: not hereditary stiff-baby syndrome
D D Weaver, D J Morley, B P Garg, et al.
American Journal of Medical Genetics
|
February 1, 1984
In utero brain destruction resulting in collapse of the fetal skull, microcephaly, scalp rugae, and neurologic impairment: the fetal brain disruption sequence
L J Russell, D D Weaver, M J Bull, et al.
Page
of 10