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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.
The New England Journal of Medicine|January 11, 1979
Duodenal-ulcer disease associated with elevated serum pepsinogen I: an inherited autosomal dominant disorderJ I Rotter, J Q Sones, I M Samloff, et al.
American Journal of Medical Genetics|January 1, 1980
Congenital macular colobomas and short-limb skeletal dysplasiaR D Smith, R M Fineman, D O Sillence, et al.
American Journal of Diseases of Children (1960)|April 1, 1982
The longitudinal study of findings in childhood. Analysis of an interdisciplinary processM D Levine, R Wolman, F Oberklaid, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|April 1, 1986
Minor neurological indicators and developmental function in preschool childrenG B Landman, M D Levine, T Fenton, et al.
American Journal of Diseases of Children (1960)|April 1, 1983
Children's descriptions of their developmental dysfunctions. Field testing of a self-administered student profileL Rappaport, M D Levine, C Aufseeser, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|April 1, 1986
Locus of control and self-esteem in children with encopresisG B Landman, L Rappaport, T Fenton, et al.
Genomics|December 1, 1993
Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19M D Briggs, I M Rasmussen, J L Weber, et al.
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