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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: kirk j. 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: kirk j. 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.
The neuroradiology of Kallmann's syndrome: a genotypic and phenotypic analysis.
Quinton R, Duke VM, de Zoysa PA, Platts AD, Valentine A, Kendall B, Pickman S, Kirk JM, Besser GM, Jacobs HS, Bouloux PM. Quinton R, et al. Among authors: kirk jm. J Clin Endocrinol Metab. 1996 Aug;81(8):3010-7. doi: 10.1210/jcem.81.8.8768867. J Clin Endocrinol Metab. 1996. PMID: 8768867 Review.
Unilateral renal aplasia in X-linked Kallmann's syndrome.
Kirk JM, Grant DB, Besser GM, Shalet S, Quinton R, Smith CS, White M, Edwards O, Bouloux PM. Kirk JM, et al. Clin Genet. 1994 Sep;46(3):260-2. doi: 10.1111/j.1399-0004.1994.tb04238.x. Clin Genet. 1994. PMID: 7820942
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: kirk jm. 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.
Sex and smell--an enigma resolved.
Bouloux PM, Munroe P, Kirk J, Besser GM. Bouloux PM, et al. Among authors: kirk j. J Endocrinol. 1992 Jun;133(3):323-6. doi: 10.1677/joe.0.1330323. J Endocrinol. 1992. PMID: 1613433 Review. No abstract available.
1,756 results