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D D Weaver

Showing results (81-90 of 99) with videos related to

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Clinical Genetics|October 1, 1984
Endocrine and genetic characterization of cousins with male pseudohermaphroditism: evidence that the Lubs phenotype can result from a mutation that alters the structure of the androgen receptorJ D Wilson, B R Carlson, D D Weaver, et al.
Clinical Genetics|November 1, 1976
Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomaliesG Higginson, D D Weaver, R E Magenis, et al.
Radiology|September 1, 1984
Type IX Ehlers-Danlos syndrome. A new variant with pathognomonic radiographic featuresD J Sartoris, L Luzzatti, D D Weaver, et al.
American Journal of Medical Genetics|December 5, 2000
Familial choanal atresia with maxillary hypoplasia, prognathism, and hypodontiaM A Ramos-Arroyo, A Valiente, E Rodriguez-Toral, et al.
American Journal of Medical Genetics|March 10, 2001
Weaver syndrome with neuroblastoma and cardiovascular anomaliesC Huffman, D McCandless, R Jasty, et al.
Human Genetics|October 1, 1986
Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literatureM J Pettenati, J L Haines, R R Higgins, et al.
American Journal of Medical Genetics|February 7, 1998
Urorectal septum malformation sequence: report of thirteen additional cases and review of the literatureP G Wheeler, D D Weaver, M O Obeime, et al.
American Journal of Human Genetics|July 1, 1993
Minimum guidelines for the delivery of clinical genetics services. The Evaluation of Clinical Services Subcommittee, Great Lakes Regional Genetics GroupD D Weaver, D Baker, M Theobald, et al.
Clinical Dysmorphology|April 18, 1998
Livedo reticularis, developmental delay and stroke-like episode in a 7-year-old maleP G Wheeler, S Medina, A Dusick, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1981
Trisomy 7 mosaicism and manifestations of Goldenhar syndrome with unilateral radial hypoplasiaM E Hodes, S Gleiser, G P DeRosa, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Clinical Genetics|October 1, 1984
Endocrine and genetic characterization of cousins with male pseudohermaphroditism: evidence that the Lubs phenotype can result from a mutation that alters the structure of the androgen receptorJ D Wilson, B R Carlson, D D Weaver, et al.
Clinical Genetics|November 1, 1976
Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomaliesG Higginson, D D Weaver, R E Magenis, et al.
Radiology|September 1, 1984
Type IX Ehlers-Danlos syndrome. A new variant with pathognomonic radiographic featuresD J Sartoris, L Luzzatti, D D Weaver, et al.
American Journal of Medical Genetics|December 5, 2000
Familial choanal atresia with maxillary hypoplasia, prognathism, and hypodontiaM A Ramos-Arroyo, A Valiente, E Rodriguez-Toral, et al.
American Journal of Medical Genetics|March 10, 2001
Weaver syndrome with neuroblastoma and cardiovascular anomaliesC Huffman, D McCandless, R Jasty, et al.
Human Genetics|October 1, 1986
Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literatureM J Pettenati, J L Haines, R R Higgins, et al.
American Journal of Medical Genetics|February 7, 1998
Urorectal septum malformation sequence: report of thirteen additional cases and review of the literatureP G Wheeler, D D Weaver, M O Obeime, et al.
American Journal of Human Genetics|July 1, 1993
Minimum guidelines for the delivery of clinical genetics services. The Evaluation of Clinical Services Subcommittee, Great Lakes Regional Genetics GroupD D Weaver, D Baker, M Theobald, et al.
Clinical Dysmorphology|April 18, 1998
Livedo reticularis, developmental delay and stroke-like episode in a 7-year-old maleP G Wheeler, S Medina, A Dusick, et al.
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1981
Trisomy 7 mosaicism and manifestations of Goldenhar syndrome with unilateral radial hypoplasiaM E Hodes, S Gleiser, G P DeRosa, et al.
Pageof 10