Unilateral renal aplasia in X-linked Kallmann's syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb04238.x/fullpdf
Reference27 articles.
1. Mullerian anomalies and renal agenesis: autosomal dominant urogenital adysplasia;Biedel;J Pediatr,1984
2. Deletion analysis maps ocular albinism proximal to the steroid sulphatase locus;Bouloux;Clin Genet,1993
3. Cortically evoked motor responses in patients with Xp22.3-linked Kallmann's syndrome and in female gene carriers;Danek;Ann Neurol,1992
4. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules;Franco;Nature,1991
5. X-linked Kallmann syndrome: stop mutations validate the ADMLX candidate gene;Hardelin;Proc Nat Acad Sci (Washington),1992
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