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Showing page 1 of results 1 - 2 of about 2 matches for "nurnberg-p"

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Familial Glucocorticoid Deficiency type 2 is associated with mutations in a novel gene encoding a small single transmembrane domain protein
LA Metherell; JP Chapple; S Cooray; C Becker; M Begeot; D Naville; P Nurnberg; A Huebner; ME Cheetham; AJL Clark
http://www.endocrine-abstracts.org/ea/0008/ea0008p83.htm
Published: 2004-11-01

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Linkage of a fourth gene for familial glucocorticoid deficiency to chromosome 13q
LA Metherell; C Becker; F Ruschendorf; D Naville; M Begeot; P Nurnberg; A Huebner; MO Savage; AJL Clark
http://www.endocrine-abstracts.org/ea/0011/ea0011oc42.htm
Published: 2006-12-04

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