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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 10, 2024. (Total: 231322Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Kallmann Syndrome and NELF[original query]
Molecular analysis of KAL-1, GnRH-R, NELF and EBF2 genes in a series of Kallmann syndrome and normosmic hypogonadotropic hypogonadism patients.
The Journal of endocrinology 2006 1 187 (3): 361-8.
Trarbach Ericka B, Baptista Maria T M, Garmes Heraldo M, Hackel Christi
Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1.
Clinical endocrinology 2010 Mar 72 (3): 371-6.
Trarbach Ericka Barbosa, Teles Milena Gurgel, Costa Elaine Maria Frade, Abreu Ana Paula, Garmes Heraldo Mendes, Guerra Gil, Baptista Maria Tereza Matias, de Castro Margaret, Mendonca Berenice Bilharinho, Latronico Ana Claud
Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.
Fertility and sterility 2011 Apr 95 (5): 1613-20.e1-7.
Xu Ning, Kim Hyung-Goo, Bhagavath Balasubramanian, Cho Sung-Gyu, Lee Jae Ho, Ha Kyungsoo, Meliciani Irene, Wenzel Wolfgang, Podolsky Robert H, Chorich Lynn P, Stackhouse Kathryn A, Grove Anna M H, Odom Lawrence N, Ozata Metin, Bick David P, Sherins Richard J, Kim Soo-Hyun, Cameron Richard S, Layman Lawrence
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