A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
about
Characterization of ARHGEF6, a guanine nucleotide exchange factor for Rho GTPases and a candidate gene for X-linked mental retardation: mutation screening in Börjeson-Forssman-Lehmann syndrome and MRX27Characterization of novel isoforms and evaluation of SNF2L/SMARCA1 as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26.The human obesity gene map: the 2000 update.The human obesity gene map: the 2001 update.The human obesity gene map: the 2002 update.A systematic review of genetic syndromes with obesity.The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome.The role of cephalometry in assessing velopharyngeal dysfunction in velocardiofacial syndrome.Shashi XLMR syndrome: report of a second family.Novel X-linked mental retardation syndrome with short stature maps to Xq24.The Human Obesity Gene Map: The 2004 Update
P2860
Q28187375-BC38262C-F855-492C-8B2D-0166966ACDD6Q33321333-662450C2-354C-489E-A0FA-10CB174ECB4EQ34227908-C6D09910-A364-4D7D-BD5C-0F624D266F3DQ34557274-CA168954-5327-4E46-953D-80C09C3AAB61Q35084465-1C543F51-248C-4C4A-9D86-B9010CF98F31Q39202448-70BCD91F-2817-4AC2-9E7B-B6F83E456810Q48514204-C6187025-E05A-44F7-BAAA-376DBCE9C826Q51057992-619637B3-53C4-492D-87F3-BBC01E314083Q51950344-7B7B0A60-0533-4D88-9697-296FC358F98BQ51963521-70043FA3-A0D1-4196-892B-60AAAF971392Q57316399-2F958CB8-9277-4A03-97E9-CF2A9CBC7533
P2860
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
description
2000 nî lūn-bûn
@nan
2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
@ast
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
@en
type
label
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
@ast
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
@en
prefLabel
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
@ast
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
@en
P2093
P2860
P356
P1476
A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
@en
P2093
P2860
P304
P356
10.1086/302772
P407
P577
2000-02-01T00:00:00Z