Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Spondyloepiphyseal dysplasia tarda (SEDL) is an X-linked recessive disorder characterized in affected males by short stature resulting from a growth defect of the vertebral bodies. We have extended our earlier studies by analyzing 15 families with newly identified microsatellite DNA markers; analysis of recombination events with these markers indicates that the gene responsible for SEDL is located in Xp22 between DXS 16 and DXS 987 on an interval spanning approximately 2 Mb.

Original publication

DOI

10.1007/BF00191797

Type

Journal article

Journal

Hum Genet

Publication Date

10/1995

Volume

96

Pages

407 - 410

Keywords

Chromosome Mapping, Female, Genetic Linkage, Humans, Male, Osteochondrodysplasias, Pedigree, Recombination, Genetic, X Chromosome