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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.
Communicable Diseases Intelligence|July 2, 1998
Arboviruses in the Australian region, 1990 to 1998J S Mackenzie, A K Broom, R A Hall, 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.
Cancer|August 1, 1997
The clinical significance of p21(WAF1/CIP-1) and p53 expression in pancreatic adenocarcinomaS T Dergham, M C Dugan, U S Joshi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 11, 2011
Abnormalities of the upper extremities on fetal magnetic resonance imagingS F Nemec, G Kasprian, P C Brugger, et al.
American Journal of Medical Genetics|June 1, 1990
Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type IIH J Stern, J M Graham, R S Lachman, 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.
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