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Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: Implication for the MRX locus

Although genotype-phenotype correlations in male patients with various types of nullisomy for Xp22.3 have assigned a locus for X-linked mental retardation (MRX) to an approximately 3-Mb region between DXS31 and STS, the precise location has not been determined. In this paper, we describe a 14 7/12 y...

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Main Authors: Muroya, Koji (Author) , Ogata, Tsutomu (Author) , Matsuo, Nobutake (Author) , Nagai, Toshiro (Author) , Franco, Brunella (Author) , Ballabio, Andrea (Author) , Rappold, Gudrun (Author) , Sakura, Nobiro (Author) , Fukushima, Yoshimitsu (Author)
Format: Article (Journal)
Language:English
Published: 6 September 1996
In: American journal of medical genetics
Year: 1996, Volume: 64, Issue: 4, Pages: 583-587
ISSN:1096-8628
DOI:https://doi.org/10.1002/(SICI)1096-8628(19960906)64:4<583::AID-AJMG11>3.0.CO;2-D
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/https://doi.org/10.1002/(SICI)1096-8628(19960906)64:4<583::AID-AJMG11>3.0.CO;2-D
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/%28SICI%291096-8628%2819960906%2964%3A4%3C583%3A%3AAID-AJMG11%3E3.0.CO%3B2-D
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Author Notes:Koji Muroya, Tsutomu Ogata, Nobutake Matsuo, Toshiro Nagai, Brunella Franco, Andrea Ballabio, Gudrun Rappold, Nobiro Sakura, and Yoshimitsu Fukushima

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