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American Journal of Medical Genetics|April 1, 1983
Familial agnathia-holoprosencephalyR M Pauli, J C Pettersen, S Arya, et al.
Experientia|January 15, 1979
Acetylsalicylic acid-induced morphological changes in the ductus arteriosus of the chick embryoS Ishikawa, M O Cheung, E F Gilbert, et al.
Medical and Pediatric Oncology|January 1, 1983
Leukemia presenting as central nervous disease without bone marrow involvementD J Ganick, P M Sondel, E F Gilbert, et al.
Archives of Biochemistry and Biophysics|July 24, 1998
Incorporation of structurally defective type II collagen into cartilage matrix in kniest chondrodysplasiaR J Fernandes, D J Wilkin, M A Weis, et al.
Birth Defects Original Article Series|January 1, 1976
Heterogeneity in the campomelic syndromes: long and short bone varietiesA Khajavi, R S Lachman, D L Rimoin, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 31, 2004
RNA oligonucleotide synthesis via 5'-silyl-2'-orthoester chemistryStephanie A Hartsel, David E Kitchen, Stephen A Scaringe, et al.
American Journal of Medical Genetics|December 8, 1998
Radiographic and morphologic findings in a previously undescribed type of mesomelic dysplasia resembling atelosteogenesis type IIS G Brodie, R S Lachman, B F Crandall, et al.
American Journal of Medical Genetics|April 11, 1991
Deletion of 20p 11.23----pter with normal growth hormone-releasing hormone genesM Shohat, V Herman, S Melmed, et al.
American Journal of Human Genetics|February 1, 1995
An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2A1) in a family with spondyloepiphyseal dysplasia congenitaG E Tiller, M A Weis, P A Polumbo, et al.
Human Molecular Genetics|February 1, 1995
A radiographic, morphologic, biochemical and molecular analysis of a case of achondrogenesis type II resulting from substitution for a glycine residue (Gly691-->Arg) in the type II collagen trimerG R Mortier, D J Wilkin, W R Wilcox, et al.
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