Analysis of an interstitial deletion in a patient with Kallmann syndrome, X-linked ichthyosis and mental retardation
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1998.tb03692.x/fullpdf
Reference38 articles.
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2. Cloning of the gene for ocular albinism type 1 from the distal short arm of the X-chromosome;Bassi;Nat Genet,1995
3. Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism;Meindl;J Med Genet,1993
4. X-chromosome-linked Kallmann's syndrome: pathology at the molecular level;Prager;J Clin Endocrinol Metab,1993
5. Origin of luteinizing hormone-releasing hormone neurons;Schwanzel-Fukuda;Nature,1989
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