Layman LC - Search Results

1

The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Kim HG, Layman LC. Kim HG, et al. Among authors: layman lc. Mol Cell Endocrinol. 2011 Oct 22;346(1-2):74-83. doi: 10.1016/j.mce.2011.07.013. Epub 2011 Aug 2. Mol Cell Endocrinol. 2011. PMID: 21856375 Free PMC article. Review.

2

The molecular basis of human hypogonadotropic hypogonadism.

Layman LC. Layman LC. Mol Genet Metab. 1999 Oct;68(2):191-9. doi: 10.1006/mgme.1999.2912. Mol Genet Metab. 1999. PMID: 10527669 Review.

3

Mutation analysis of the EMX2 gene in Kallmann's syndrome.

Taylor HS, Block K, Bick DP, Sherins RJ, Layman LC. Taylor HS, et al. Among authors: layman lc. Fertil Steril. 1999 Nov;72(5):910-4. doi: 10.1016/s0015-0282(99)00376-3. Fertil Steril. 1999. PMID: 10560999 Free article.

4

Genetics of human hypogonadotropic hypogonadism.

Layman LC. Layman LC. Am J Med Genet. 1999 Dec 29;89(4):240-8. doi: 10.1002/(sici)1096-8628(19991229)89:4<240::aid-ajmg8>3.0.co;2-7. Am J Med Genet. 1999. PMID: 10727999 Review.

5

Mutations of follicle stimulating hormone-beta and its receptor in human and mouse: genotype/phenotype.

Layman LC, McDonough PG. Layman LC, et al. Mol Cell Endocrinol. 2000 Mar 30;161(1-2):9-17. doi: 10.1016/s0303-7207(99)00217-8. Mol Cell Endocrinol. 2000. PMID: 10773385 Review.

6

The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism.

Bhagavath B, Ozata M, Ozdemir IC, Bolu E, Bick DP, Sherins RJ, Layman LC. Bhagavath B, et al. Among authors: layman lc. Fertil Steril. 2005 Oct;84(4):951-7. doi: 10.1016/j.fertnstert.2005.04.029. Fertil Steril. 2005. PMID: 16213849

7

Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism.

Bhagavath B, Podolsky RH, Ozata M, Bolu E, Bick DP, Kulharya A, Sherins RJ, Layman LC. Bhagavath B, et al. Among authors: layman lc. Fertil Steril. 2006 Mar;85(3):706-13. doi: 10.1016/j.fertnstert.2005.08.044. Fertil Steril. 2006. PMID: 16500342 Free article.

8

A mutation in the fibroblast growth factor receptor 1 gene causes fully penetrant normosmic isolated hypogonadotropic hypogonadism.

Xu N, Qin Y, Reindollar RH, Tho SP, McDonough PG, Layman LC. Xu N, et al. Among authors: layman lc. J Clin Endocrinol Metab. 2007 Mar;92(3):1155-8. doi: 10.1210/jc.2006-1183. Epub 2007 Jan 2. J Clin Endocrinol Metab. 2007. PMID: 17200176

9

KAL1 mutations are not a common cause of idiopathic hypogonadotrophic hypogonadism in humans.

Bhagavath B, Xu N, Ozata M, Rosenfield RL, Bick DP, Sherins RJ, Layman LC. Bhagavath B, et al. Among authors: layman lc. Mol Hum Reprod. 2007 Mar;13(3):165-70. doi: 10.1093/molehr/gal108. Epub 2007 Jan 9. Mol Hum Reprod. 2007. PMID: 17213338

10

Hypogonadotropic hypogonadism.

Layman LC. Layman LC. Endocrinol Metab Clin North Am. 2007 Jun;36(2):283-96. doi: 10.1016/j.ecl.2007.03.010. Endocrinol Metab Clin North Am. 2007. PMID: 17543719 Review.

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