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The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Somatic mutations in MEN type 1 tumors, consistent with the Knudson "two-hit" hypothesisA A Pannett, R V ThakkerHuman Genetics|June 1, 1995
Highly polymorphic sequence at D21S1448 mapping close to D21S55, within the Down syndrome critical regionD Hernandez, A A Pannett, V Tybulewicz, et al.American Journal of Human Genetics|January 23, 1999
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13S E Lloyd, A A Pannett, P H Dixon, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 20, 1999
Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1J H Bassett, P Rashbass, B Harding, et al.Journal of Medical Genetics|August 1, 1997
Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36C Williamson, A A Pannett, J T Pang, et al.The Journal of Clinical Endocrinology and Metabolism|September 22, 2000
A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindredS Mumm, P T Christie, P Finnegan, et al.Biochemical and Biophysical Research Communications|August 14, 2001
Menin interacts directly with the homeobox-containing protein PemI H Lemmens, L Forsberg, A A Pannett, et al.QJM : Monthly Journal of the Association of Physicians|April 11, 2001
The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindredB M Cavaco, L Barros, A A Pannett, et al.Genomics|November 1, 1996
Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1)A Courseaux, J Grosgeorge, P Gaudray, et al.Pageof 2