Literature DB >> 8826466

How many X-linked genes for non-specific mental retardation (MRX) are there?

A K Gedeon, A J Donnelly, J C Mulley, B Kerr, G Turner.   

Abstract

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Year:  1996        PMID： 8826466     DOI： 10.1002/(SICI)1096-8628(19960712)64:1<158::AID-AJMG26>3.0.CO;2-L

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  16 in total

1.  Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11.

Authors:  K Muroya; E Kinoshita; T Kamimaki; N Matsuo; T Yorifugi; T Ogata
Journal:  J Med Genet       Date:  1999-03       Impact factor: 6.318

2.  A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.

Authors:  G S Pai; B Hane; M Joseph; R Nelson; L S Hammond; J F Arena; H A Lubs; R E Stevenson; C E Schwartz
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

3.  Identification and characterization of proSAAS, a granin-like neuroendocrine peptide precursor that inhibits prohormone processing.

Authors:  L D Fricker; A A McKinzie; J Sun; E Curran; Y Qian; L Yan; S D Patterson; P L Courchesne; B Richards; N Levin; N Mzhavia; L A Devi; J Douglass
Journal:  J Neurosci       Date:  2000-01-15       Impact factor: 6.167

4.  A family with mental retardation, variable macrocephaly and macro-orchidism, and linkage to Xq12-q21.

Authors:  J P Johnson; R Nelson; C E Schwartz
Journal:  J Med Genet       Date:  1998-12       Impact factor: 6.318

5.  Renpenning syndrome maps to Xp11.

Authors:  R E Stevenson; J F Arena; E Ouzts; A Gibson; M H Shokeir; C Vnencak-Jones; H A Lubs; M May; C E Schwartz
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025

6.  A gene for dominant nonspecific X-linked mental retardation is located in Xq28.

Authors:  V des Portes; P Billuart; A Carrié; L Bachner; T Bienvenu; M C Vinet; C Beldjord; G Ponsot; A Kahn; J Boué; J Chelly
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

7.  Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation.

Authors:  Olivier Hagens; Aline Dubos; Fatima Abidi; Gotthold Barbi; Laura Van Zutven; Maria Hoeltzenbein; Niels Tommerup; Claude Moraine; Jean-Pierre Fryns; Jamel Chelly; Hans van Bokhoven; Jozef Gécz; Hélène Dollfus; Hans-Hilger Ropers; Charles E Schwartz; Rita de Cassia Stocco Dos Santos; Vera Kalscheuer; André Hanauer
Journal:  Hum Genet       Date:  2005-10-26       Impact factor: 4.132

8.  A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.

Authors:  V Shashi; M N Berry; S Shoaf; J J Sciote; D Goldstein; T C Hart
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

9.  Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.

Authors:  D Lugtenberg; A P M de Brouwer; T Kleefstra; A R Oudakker; S G M Frints; C T R M Schrander-Stumpel; J P Fryns; L R Jensen; J Chelly; C Moraine; G Turner; J A Veltman; B C J Hamel; B B A de Vries; H van Bokhoven; H G Yntema
Journal:  J Med Genet       Date:  2005-09-16       Impact factor: 6.318

10.  Localisation of a gene for non-specific X linked mental retardation (MRX46) to Xq25-q26.

Authors:  H G Yntema; B C Hamel; A P Smits; T van Roosmalen; B van den Helm; H Kremer; H H Ropers; D F Smeets; H van Bokhoven
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318
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