about
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationMutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation.The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardationThe apolipoprotein E gene, attention, and brain functionMutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardationNutritional status, brain development and scholastic achievement of Chilean high-school graduates from high and low intellectual quotient and socio-economic statusNovel mental retardation-epilepsy syndrome linked to Xp21.1-p11.4.In search of the MRX genes.X linked mental retardation: a clinical guide.Dietary patterns in pregnancy and effects on nutrient intake in the Mid-South: the Conditions Affecting Neurocognitive Development and Learning in Early Childhood (CANDLE) study.Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations.A comparative expression analysis of four MRX genes regulating intracellular signalling via small GTPases.Novel intragenic deletion in OPHN1 in a family causing XLMR with cerebellar hypoplasia and distinctive facial appearance.A Role for the X Chromosome in Sex Differences in Variability in General Intelligence?The relative contribution of the X chromosome to ocular phenotypes.Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardation.Localization of a non-syndromic X-linked mental retardation gene (MRX80) to Xq22-q24.X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3.Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.Genetic services for people with intellectual disability and their families.Early childhood cognitive development is affected by interactions among illness, diet, enteropathogens and the home environment: findings from the MAL-ED birth cohort study
P2860
Q22254646-EADEC188-EB17-4229-AE8C-C7008960B2A6Q24534092-DE3C37C7-D83B-4166-AE9B-0378F93B8734Q24535650-8F738953-CE57-45DC-B72D-D0D57A02250BQ24539024-7DFFC25A-475B-4858-AF33-0B54FE562B75Q24612060-08057A55-5A3A-49CC-BE58-0FE3CF48FF3EQ30054216-6E9415F0-BED7-41A7-9A9B-5D3799D03BB5Q34108701-AF83E99B-0D3B-445C-AD65-DB2568326EC1Q34306151-75801B03-694E-4D10-8978-E6AC082EFACAQ36239035-322EAA58-3FA8-4E2D-9A28-72F715B0ACB8Q37002522-2D8BA01C-9BDE-4A98-BE44-A4F8068C0DA2Q43804873-D816CFE6-4949-4DC7-BD29-4AB2BD285E52Q48117476-34009301-1630-472A-9668-58EDA54F19D9Q51850072-E1CFE53B-4B91-48AE-AC21-68CA68BB57B1Q51861376-D7B38EAF-AAFB-4EC6-9196-81143415BF06Q51923277-2E406F8C-D605-48C3-9F9C-1202811E82C7Q51929767-DA72F829-D07D-4F41-A19D-1FA4734409DBQ51946976-A9282712-4E78-4847-BABD-12B6845A8E87Q51947561-B152CF60-EB6D-4426-8220-E315C2156851Q51967079-4B336BEE-8798-4FC5-985B-FAD06DDC5201Q53373111-B3E7CE0C-2157-43D5-A0AB-573A5BBA63A7Q56929432-48D80380-0E22-4DA4-9EBC-A8967A3FF8D4
P2860
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
Genes for cognitive function: developments on the X.
@ast
Genes for cognitive function: developments on the X.
@en
type
label
Genes for cognitive function: developments on the X.
@ast
Genes for cognitive function: developments on the X.
@en
prefLabel
Genes for cognitive function: developments on the X.
@ast
Genes for cognitive function: developments on the X.
@en
P356
P1433
P1476
Genes for cognitive function: developments on the X.
@en
P2093
P304
P356
10.1101/GR.10.2.157
P50
P577
2000-02-01T00:00:00Z