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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 22, 2025. (Total: 235574Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Kallmann Syndrome and TACR3[original query]
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
Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism.
Journal of pediatric endocrinology & metabolism : JPEM 2017 Sep .
Aoyama Kohei, Mizuno Haruo, Tanaka Tatsushi, Togawa Takao, Negishi Yutaka, Ohashi Kei, Hori Ikumi, Izawa Masako, Hamajima Takashi, Saitoh Shin
Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2018 9 127 (8): 538-544.
Kim Ja Hye, Seo Go Hun, Kim Gu-Hwan, Huh Juyoung, Hwang Il Tae, Jang Ja-Hyun, Yoo Han-Wook, Choi Jin-
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