caa a22 4500 467984530 CHVBK 20180323112528.0 cr unu---uuuuu 170328e19900601xx s 000 0 eng 10.1007/BF00276335 doi (NATIONALLICENCE)springer-10.1007/BF00276335 DXS26 (HU16) is located in Xq21.1 [Elektronische Daten] [Eeva-Marja Sankila, Gail Bruns, Marianne Schwartz, Eeva Nikoskelainen, Erik Niebuhr, Shirley Hodgson, Alan Wright, Albert de la Chapelle] Summary: We have localized a single-copy DNA probe, HU16 (locus DXS26), to Xq21.1. The probe was isolated from a human-mouse hybrid X;13 library and mapped with human-mouse hybrids containing different portions of the human X chromosome and DNA from male patients with different X-chromosomal deletions. The following order of loci is proposed: Xcen-(DXS72, DXS169)-(DXS232,DXS26)-DXS121-DXS233-DXS165 TCD-DXS95-DXYSl-Xqter. HU16 will be useful in the study of the putative genes that reside in Xq21 and whose defects lead to deafness and mental retardation. Springer-Verlag, 1990 Sankila Eeva-Marja Department of Medical Genetics, University of Helsinki, and Folkhälsan Institute of Genetics, SF-00290, Helsinki, Finland aut Bruns Gail Departments of Pediatrics and Genetics, Harvard Medical School, 02115, Boston, MA, USA aut Schwartz Marianne Section of Clinical Genetics 4062, Department of Pediatrics, Rigshospitalet, DK-2100, Copenhagen, Denmark aut Nikoskelainen Eeva Department of Ophthalmology, University of Turku, SF-20520, Turku, Finland aut Niebuhr Erik Institute of Medical Genetics, University of Copenhagen, DK-2200, Copenhagen, Denmark aut Hodgson Shirley Pediatric Research Unit, United Medical and Dental Schools of Guy's and St.Thomas's Hospitals, SE1 9RT, London, UK aut Wright Alan MRC Human Genetics Unit, Western General Hospital, EH4 2XU, Edinburgh, UK aut de la Chapelle Albert Department of Medical Genetics, University of Helsinki, and Folkhälsan Institute of Genetics, SF-00290, Helsinki, Finland aut Human Genetics Springer-Verlag 85/1(1990-06-01), 117-120 0340-6717 85:1<117 1990 85 439 https://doi.org/10.1007/BF00276335 text/html Onlinezugriff via DOI 1 brief-communication jats NATIONALLICENCE 856 40 https://doi.org/10.1007/BF00276335 text/html Onlinezugriff via DOI NATIONALLICENCE 700 1- Sankila Eeva-Marja Department of Medical Genetics, University of Helsinki, and Folkhälsan Institute of Genetics, SF-00290, Helsinki, Finland aut NATIONALLICENCE 700 1- Bruns Gail Departments of Pediatrics and Genetics, Harvard Medical School, 02115, Boston, MA, USA aut NATIONALLICENCE 700 1- Schwartz Marianne Section of Clinical Genetics 4062, Department of Pediatrics, Rigshospitalet, DK-2100, Copenhagen, Denmark aut NATIONALLICENCE 700 1- Nikoskelainen Eeva Department of Ophthalmology, University of Turku, SF-20520, Turku, Finland aut NATIONALLICENCE 700 1- Niebuhr Erik Institute of Medical Genetics, University of Copenhagen, DK-2200, Copenhagen, Denmark aut NATIONALLICENCE 700 1- Hodgson Shirley Pediatric Research Unit, United Medical and Dental Schools of Guy's and St.Thomas's Hospitals, SE1 9RT, London, UK aut NATIONALLICENCE 700 1- Wright Alan MRC Human Genetics Unit, Western General Hospital, EH4 2XU, Edinburgh, UK aut NATIONALLICENCE 700 1- de la Chapelle Albert Department of Medical Genetics, University of Helsinki, and Folkhälsan Institute of Genetics, SF-00290, Helsinki, Finland aut NATIONALLICENCE 773 0- Human Genetics Springer-Verlag 85/1(1990-06-01), 117-120 0340-6717 85:1<117 1990 85 439 Metadata rights reserved Springer special CC-BY-NC licence nationallicence BK010053 XK010053 XK010000 NATIONALLICENCE NATIONALLICENCE NL-springer