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D D Weaver

Showing results (41-50 of 99) with videos related to

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The Journal of Pediatrics|March 1, 1990
Fetal brain disruption sequenceC A Moore, D D Weaver, M J Bull
Journal of Medical Genetics|September 1, 1974
The tricho-rhino-phalangeal syndromeD D Weaver, M M Cohen, D W Smith
American Journal of Diseases of Children (1960)|March 1, 1986
The VATER association. Analysis of 46 patientsD D Weaver, C L Mapstone, P L Yu
Clinical Genetics|June 1, 1985
Congenital contractural arachnodactyly. Report of four additional families and review of literatureM 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 carrierI 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 casesK Young, C K Barth, C Moore, et al.
Human Genetics|January 1, 1983
Dicentric chromosome 13 and centromere inactivationS Schwartz, C G Palmer, D D Weaver, et al.
Pediatrics|December 1, 1991
Weaver syndrome: a case without early overgrowth and review of the literatureM A Ramos-Arroyo, D D Weaver, E R Banks
American Journal of Diseases of Children (1960)|June 1, 1982
Hyperexplexia: not hereditary stiff-baby syndromeD 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 sequenceL J Russell, D D Weaver, M J Bull, et al.
Pageof 10

Showing results (41-50 of 99) with videos related to

Sort By:
Pageof 10
The Journal of Pediatrics|March 1, 1990
Fetal brain disruption sequenceC A Moore, D D Weaver, M J Bull
Journal of Medical Genetics|September 1, 1974
The tricho-rhino-phalangeal syndromeD D Weaver, M M Cohen, D W Smith
American Journal of Diseases of Children (1960)|March 1, 1986
The VATER association. Analysis of 46 patientsD D Weaver, C L Mapstone, P L Yu
Clinical Genetics|June 1, 1985
Congenital contractural arachnodactyly. Report of four additional families and review of literatureM 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 carrierI 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 casesK Young, C K Barth, C Moore, et al.
Human Genetics|January 1, 1983
Dicentric chromosome 13 and centromere inactivationS Schwartz, C G Palmer, D D Weaver, et al.
Pediatrics|December 1, 1991
Weaver syndrome: a case without early overgrowth and review of the literatureM A Ramos-Arroyo, D D Weaver, E R Banks
American Journal of Diseases of Children (1960)|June 1, 1982
Hyperexplexia: not hereditary stiff-baby syndromeD 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 sequenceL J Russell, D D Weaver, M J Bull, et al.
Pageof 10