Loading…
Loading…
Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy
Dorboz, Imen, Aiello, Chiara, Simons, Cas, Stone, Robert Thompson, Niceta, Marcello, Elmaleh, Monique, Abuawad, Mohammad, Doummar, Diane, Bruselles, Alessandro, Wolf, Nicole I, Travaglini, Lorena, Boespflug-Tanguy, Odile, Tartaglia, Marco, Vanderver, Adeline, Rodriguez, Diana, Bertini, Enrico
Published in Brain (London, England : 1878) (01.10.2017)
Published in Brain (London, England : 1878) (01.10.2017)
Get full text
Journal Article
Loading…
survey of genes differentially expressed in subcutaneous and visceral adipose tissue in men
Vohl, M.C, Sladek, R, Robitaille, J, Gurd, S, Marceau, P, Richard, D, Hudson, T.J, Tchernof, A
Published in Obesity (Silver Spring, Md.) (01.08.2004)
Published in Obesity (Silver Spring, Md.) (01.08.2004)
Get full text
Journal Article
Loading…
HOX gene methylation status analysis in patients with hereditary breast cancer
Pilato, Brunella, Pinto, Rosamaria, De Summa, Simona, Lambo, Rossana, Paradiso, Angelo, Tommasi, Stefania
Published in Journal of human genetics (01.01.2013)
Published in Journal of human genetics (01.01.2013)
Get full text
Journal Article
Loading…
Loading…
Loading…
Eight-alanine duplication in homeobox D13 in a Chinese family with synpolydactyly
Xin, Qian, Li, Lin, Li, Jiangxia, Qiu, Rongfang, Guo, Chenhong, Gong, Yaoqin, Liu, Qiji
Published in Gene (10.05.2012)
Published in Gene (10.05.2012)
Get full text
Journal Article
Loading…
Loading…
Loading…
An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
Baldwin, Clinton T., Hoth, Christopher F., Amos, Jean A., da-Silva, Elias O., Milunsky, Aubrey
Published in Nature (London) (13.02.1992)
Published in Nature (London) (13.02.1992)
Get full text
Journal Article
Loading…
Loading…
Protein evolution of ANTP and PRD homeobox genes
Fonseca, Nuno A, Vieira, Cristina P, Holland, Peter WH, Vieira, Jorge
Published in BMC evolutionary biology (11.07.2008)
Published in BMC evolutionary biology (11.07.2008)
Get full text
Journal Article
Loading…
Loading…
Loading…
A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families
Price, J A, Wright, J T, Kula, K, Bowden, D W, Hart, T C
Published in Journal of medical genetics (01.10.1998)
Published in Journal of medical genetics (01.10.1998)
Get full text
Journal Article
Loading…
Cerebellum development and schizophrenia: an association study of the human homeogene Engrailed 2
Gourion, David, Leroy, Sophie, Bourdel, Marie-Chantal, Goldberger, Céline, Poirier, Marie-France, Olié, Jean-Pierre, Krebs, Marie-Odile
Published in Psychiatry research (30.04.2004)
Published in Psychiatry research (30.04.2004)
Get full text
Journal Article
Loading…
Comparative analysis of leg and antenna development in wild-type and homeotic Drosophila melanogaster
Cummins, Mark, Pueyo, Jose I., Greig, Steve A., Couso, Juan Pablo
Published in Development Genes and Evolution (01.07.2003)
Published in Development Genes and Evolution (01.07.2003)
Get full text
Journal Article
Loading…
Analysis of homeobox gene HOXA10 mutations in cryptorchidism
Kolon, T F, Wiener, J S, Lewitton, M, Roth, D R, Gonzales, Jr, E T, Lamb, D J
Published in The Journal of urology (01.01.1999)
Published in The Journal of urology (01.01.1999)
Get more information
Journal Article