Necdin, a PraderWilli syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development

By Miller Nichol L.G.   Wevrick Rachel   Mellon Pamela L.  

Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. : 248-260

Oxford University Press

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The product of X-linked Kallmann's syndrome gene ( KAL1 ) affects the migratory activity of gonadotropin-releasing hormone (GnRH)-producing neurons

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Human Molecular Genetics, Vol. 13, Iss. 22, 2004-11 ,pp. : 2781-2791

Oxford University Press

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Defective gonadotropin-releasing hormone neuron migration in mice lacking SEMA3A signalling through NRP1 and NRP2: implications for the aetiology of hypogonadotropic hypogonadism

By Cariboni Anna   Davidson Kathryn   Rakic Sonja   Maggi Roberto   Parnavelas John G.   Ruhrberg Christiana  

Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 336-344

Oxford University Press

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A regulatory SNP of the BICD1 gene contributes to telomere length variation in humans

By Mangino Massimo   Brouilette Scott   Braund Peter   Tirmizi Nighat   Vasa-Nicotera Mariuca   Thompson John R.   Samani Nilesh J.  

Human Molecular Genetics, Vol. 17, Iss. 16, 2008-08 ,pp. : 2518-2523

Oxford University Press

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A hypomorphic Artemis human disease allele causes aberrant chromosomal rearrangements and tumorigenesis

By Jacobs Cheryl   Huang Ying   Masud Tehmina   Lu William   Westfield Gerwin   Giblin William   Sekiguchi JoAnn M.  

Human Molecular Genetics, Vol. 20, Iss. 4, 2011-02 ,pp. : 806-819

Oxford University Press

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