Search research articles
Contact Us
Filters
Showing results (81-90 of 99) with videos related to
Page
of 10
Sort By:
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 receptor
J 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 anomalies
G Higginson, D D Weaver, R E Magenis, et al.
Radiology
|
September 1, 1984
Type IX Ehlers-Danlos syndrome. A new variant with pathognomonic radiographic features
D 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 hypodontia
M A Ramos-Arroyo, A Valiente, E Rodriguez-Toral, et al.
American Journal of Medical Genetics
|
March 10, 2001
Weaver syndrome with neuroblastoma and cardiovascular anomalies
C 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 literature
M 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 literature
P 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 Group
D 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 male
P 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 hypoplasia
M E Hodes, S Gleiser, G P DeRosa, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 99) with videos related to
Sort By:
Page
of 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 receptor
J 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 anomalies
G Higginson, D D Weaver, R E Magenis, et al.
Radiology
|
September 1, 1984
Type IX Ehlers-Danlos syndrome. A new variant with pathognomonic radiographic features
D 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 hypodontia
M A Ramos-Arroyo, A Valiente, E Rodriguez-Toral, et al.
American Journal of Medical Genetics
|
March 10, 2001
Weaver syndrome with neuroblastoma and cardiovascular anomalies
C 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 literature
M 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 literature
P 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 Group
D 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 male
P 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 hypoplasia
M E Hodes, S Gleiser, G P DeRosa, et al.
Page
of 10