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American Journal of Medical Genetics
|
August 1, 1982
Limb pterygium syndromes: a review and report of eleven patients
J G Hall, S D Reed, K N Rosenbaum, et al.
American Journal of Medical Genetics
|
January 1, 1989
De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome
D Chitayat, C L Fagerstrom, D K Kalousek, et al.
Clinical Genetics
|
February 1, 1982
Three distinct types of X-linked arthrogryposis seen in 6 families
J G Hall, S D Reed, C I Scott, et al.
The New England Journal of Medicine
|
July 10, 1980
X-linked cutis laxa: defective cross-link formation in collagen due to decreased lysyl oxidase activity
P H Byers, R C Siegel, K A Holbrook, et al.
American Journal of Human Genetics
|
January 1, 1979
Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes
R A Pagon, J G Hall, S L Davenport, et al.
Annals of Human Genetics
|
January 1, 1970
Achondroplasia--a genetic and statistical survey
J L Murdoch, B A Walker, J G Hall, et al.
American Journal of Medical Genetics
|
January 1, 1979
Failure to early prenatal diagnosis in classic achondroplasia
J G Hall, M S Golbus, C B Graham, et al.
American Journal of Medical Genetics
|
October 28, 1996
Segregation analysis of microcephaly
T Cohen, M Zeitune, B C McGillivray, et al.
American Journal of Medical Genetics
|
April 1, 1987
Dominantly inherited renal adysplasia
E McPherson, J Carey, A Kramer, et al.
Journal of Immunological Methods
|
September 30, 1982
Production of IgA secreting hybridomas: a monoclonal rat antibody of the IgA class with specificity for RT1c
C J Dean, L A Gyure, J M Styles, et al.
Page
of 43
Search research articles
Search
Showing results (361-370 of 426) with videos related to
Sort By:
Page
of 43
American Journal of Medical Genetics
|
August 1, 1982
Limb pterygium syndromes: a review and report of eleven patients
J G Hall, S D Reed, K N Rosenbaum, et al.
American Journal of Medical Genetics
|
January 1, 1989
De novo reciprocal 1p;2q translocation in a child with multiple congenital anomalies/mental retardation syndrome
D Chitayat, C L Fagerstrom, D K Kalousek, et al.
Clinical Genetics
|
February 1, 1982
Three distinct types of X-linked arthrogryposis seen in 6 families
J G Hall, S D Reed, C I Scott, et al.
The New England Journal of Medicine
|
July 10, 1980
X-linked cutis laxa: defective cross-link formation in collagen due to decreased lysyl oxidase activity
P H Byers, R C Siegel, K A Holbrook, et al.
American Journal of Human Genetics
|
January 1, 1979
Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes
R A Pagon, J G Hall, S L Davenport, et al.
Annals of Human Genetics
|
January 1, 1970
Achondroplasia--a genetic and statistical survey
J L Murdoch, B A Walker, J G Hall, et al.
American Journal of Medical Genetics
|
January 1, 1979
Failure to early prenatal diagnosis in classic achondroplasia
J G Hall, M S Golbus, C B Graham, et al.
American Journal of Medical Genetics
|
October 28, 1996
Segregation analysis of microcephaly
T Cohen, M Zeitune, B C McGillivray, et al.
American Journal of Medical Genetics
|
April 1, 1987
Dominantly inherited renal adysplasia
E McPherson, J Carey, A Kramer, et al.
Journal of Immunological Methods
|
September 30, 1982
Production of IgA secreting hybridomas: a monoclonal rat antibody of the IgA class with specificity for RT1c
C J Dean, L A Gyure, J M Styles, et al.
Page
of 43