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Histopathological Basis of Hearing Impairment in Wolf-Hirschhorn Syndrome

โœ Scribed by Seckin O. Ulualp; Charles G. Wright; Karen S. Pawlowski; Peter S. Roland


Book ID
110085815
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
978 KB
Volume
114
Category
Article
ISSN
0023-852X

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Parental origin of chromosome 4p deletio
โœ Dallapiccola, Bruno ;Mandich, Paola ;Bellone, Emilia ;Selicorni, Angelo ;Mokin, ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 338 KB ๐Ÿ‘ 2 views

## Abstract We report on molecular studies in 7 patients with Wolfโ€Hirschhorn syndrome (WHC) not showing an obvious chromosome 4p deletion. Analysis of a set of polymorphic probes mapping in the 4p16.3 region showed the absence of paternal haplotypes in 5 cases, and maternal haplotypes in 2. These