Mental Retardation and Abnormal Skeletal Development (Dyggve-Melchior-Clausen Dysplasia) Due to Mutations in a Novel, Evolutionarily Conserved Gene
The American Journal of Human Genetics2003Vol. 72(2), pp. 419–428
Citations Over TimeTop 22% of 2003 papers
Daniel H. Cohn, Nadia Ehtesham, Deborah Krakow, Sheila Unger, Alan Shanske, Kent A. Reinker, Berkley R. Powell, David L. Rimoin
Related Papers
- → FRAMESHIFT SUPPRESSION IN SACCHAROMYCES CEREVISIAE. II. GENETIC PROPERTIES OF GROUP II SUPPRESSORS(1980)95 cited
- → Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients(1994)44 cited
- → A frameshift insertion in the cone cyclic nucleotide gated cation channel causes complete achromatopsia in a consanguineous family from a rural isolate(2002)29 cited
- → FRAMESHIFT SUPPRESSION IN SACCHAROMYCES CEREVISIAE. V. ISOLATION AND GENETIC PROPERTIES OF NONGROUP-SPECIFIC SUPPRESSORS(1982)34 cited
- → Identification of a Novel KRT9 Frameshift Mutation in a Chinese Pedigree with Epidermolytic Palmoplantar Keratoderma(2021)