Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323

Abstract

Journal Article Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323 Get access Thomas W. Glover, Thomas W. Glover * *To whom correspondence should be addressed at: Department of Human Genetics, 4708 Med. Sci II, Box 0618, University of Michigan, Ann Arbor, MI 48109, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Vera Verga, Vera Verga Search for other works by this author on: Oxford Academic PubMed Google Scholar Jill Rafael, Jill Rafael Search for other works by this author on: Oxford Academic PubMed Google Scholar Christine Barcroft, Christine Barcroft Search for other works by this author on: Oxford Academic PubMed Google Scholar Jerome L. Gorski, Jerome L. Gorski Search for other works by this author on: Oxford Academic PubMed Google Scholar Erawati V. Bawle, Erawati V. Bawle 1Department of Genetics and Metabolic Disorders, Detroit Children's HospitalDetroit, MI Search for other works by this author on: Oxford Academic PubMed Google Scholar James V. Higgins James V. Higgins 2Department of Pediatrics and Human Development, Michigan State UnivesityE Lanang, MI, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 2, Issue 10, October 1993, Pages 1717–1718, https://doi.org/10.1093/hmg/2.10.1717 Published: 01 October 1993 Article history Received: 21 June 1993 Revision received: 08 August 1993 Accepted: 08 August 1993 Published: 01 October 1993