Literature DB >> 7581391

Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM.

M May1, L Colleaux, A Murgia, A Aylsworth, R Nussbaum, M Fontes, C Schwartz.   

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Year:  1995        PMID： 7581391     DOI： 10.1093/hmg/4.8.1465

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN： 0964-6906            Impact factor:   6.150


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  3 in total

1.  Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1.

Authors:  L Villard; S Briault; A M Lossi; C Paringaux; J Belougne; L Colleaux; D R Pincus; E Woollatt; J Lespinasse; A Munnich; C Moraine; M Fontès; J Gecz
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

2.  Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH.

Authors:  F Sloan-Béna; C Philippe; B LeHeup; F Wuilque; E R Levy; M Chéry; P Jonveaux; A P Monaco
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

3.  Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711.

Authors:  Jiyong Wang; Aidin Foroutan; Ellen Richardson; Steven A Skinner; Jack Reilly; Jennifer Kerkhof; Cynthia J Curry; Patrick S Tarpey; Stephen P Robertson; Isabelle Maystadt; Boris Keren; Joanne W Dixon; Cindy Skinner; Rachel Stapleton; Lyse Ruaud; Evren Gumus; Phillis Lakeman; Mariëlle Alders; Matthew L Tedder; Charles E Schwartz; Michael J Friez; Bekim Sadikovic; Roger E Stevenson
Journal:  Eur J Hum Genet       Date:  2022-01-07       Impact factor: 4.246
  3 in total

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