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American Journal of Medical Genetics|May 1, 1989
Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndromeU Tantravahi, R D Nicholls, H Stroh, et al.American Journal of Human Genetics|January 11, 1991
Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasiaJ E Finkelstein, K Doege, Y Yamada, et al.Journal of Medical Genetics|November 1, 1996
Exclusion of candidate loci and cholesterol biosynthetic abnormalities in familial Pallister-Hall syndromeL G Biesecker, S Kang, A A Schäffer, et al.American Journal of Human Genetics|August 11, 1991
Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15J Wagstaff, J H Knoll, J Fleming, et al.American Journal of Medical Genetics|May 1, 1989
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndromeR D Nicholls, J H Knoll, K Glatt, et al.American Journal of Medical Genetics|May 2, 1997
Deletions of 20p12 in Alagille syndrome: frequency and molecular characterizationI D Krantz, E B Rand, A Genin, et al.American Journal of Medical Genetics. Part A|June 9, 2005
The adult phenotype in Costello syndromeSusan M White, J M Graham, B Kerr, et al.American Journal of Human Genetics|March 31, 2000
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) geneL B Meira, J M Graham, C R Greenberg, et al.Clinical Genetics|July 9, 2013
Phenotype-genotype correlations in patients with Marinesco-Sjögren syndromeF Ezgu, P Krejci, S Li, et al.Genomics|August 11, 1992
Deletion mapping of H-Y antigen to the long arm of the human Y chromosomeM A Cantrell, J S Bogan, E Simpson, et al.Pageof 42