Mammalian Genome 12, 796–798 (2001). DOI: 10.1007/s00335-001-1006-5 Incorporating Mouse Genome © Springer-Verlag New York Inc. 2001 Analysis of Mid1, Hccs, Arhgap6, and Msl3l1 in X-linked polydactyly (Xpl) and Patchy-fur (Paf) mutant mice 1 2 1 1,3,4 Trena A. Cormier, * Siddharth K. Prakash, * Daniel B. Magner, Huda Y. Zoghbi, 1,5 Ignatia B. Van den Veyver Interdepartmental Program in Cell and Molecular Biology, Baylor College of Medicine, Houston, TX 77030, USA Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA Howard Hughes Medical Institute, Baylor College of Medicine, Houston, TX 77030, USA Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA Department of Obstetrics and Gynecology, Baylor College of Medicine, 6550 Fannin, Suite 901, Houston, TX 77030, USA Received: 26 March 2001 / Accepted: 7 June 2001 Our laboratory has a long-standing interest in human developmen- Prakash et al. 1999). To investigate the functions of the candidate tal disorders that are caused by defects in Xp22.3, including mi- genes and their roles in MLS syndrome or in other neurodevelop- crophthalmia with linear skin defects (MLS, McKusick 309801), mental disorders linked to Xp22, we searched for potential mouse which is characterized by microphthalmia,
Mammalian Genome – Springer Journals
Published: Feb 20, 2014
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