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Xp22.3 deletions in isolated familial Kallmann's syndrome.
Hardelin JP, Levilliers J, Young J, Pholsena M, Legouis R, Kirk J, Bouloux P, Petit C, Schaison G. Hardelin JP, et al. Among authors: legouis r. J Clin Endocrinol Metab. 1993 Apr;76(4):827-31. doi: 10.1210/jcem.76.4.8473391. J Clin Endocrinol Metab. 1993. PMID: 8473391
X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene.
Hardelin JP, Levilliers J, del Castillo I, Cohen-Salmon M, Legouis R, Blanchard S, Compain S, Bouloux P, Kirk J, Moraine C, et al. Hardelin JP, et al. Among authors: legouis r. Proc Natl Acad Sci U S A. 1992 Sep 1;89(17):8190-4. doi: 10.1073/pnas.89.17.8190. Proc Natl Acad Sci U S A. 1992. PMID: 1518845 Free PMC article.
A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3).
Bouloux PM, Hardelin JP, Munroe P, Kirk JM, Legouis R, Levilliers J, Hazan J, Weissenbach J, Petit C. Bouloux PM, et al. Among authors: legouis r. Nucleic Acids Res. 1991 Oct 11;19(19):5453. doi: 10.1093/nar/19.19.5453. Nucleic Acids Res. 1991. PMID: 1923841 Free PMC article.
59 results