about
X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation.Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35).Tuber cinereum diverticula in a 28-month-old with xq21 deletion syndrome.Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without alpha-thalassemia
P2860
description
1993 nî lūn-bûn
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1993年の論文
@ja
1993年学术文章
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1993年学术文章
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1993年学术文章
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1993年学术文章
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1993年学术文章
@zh-my
1993年学术文章
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1993年學術文章
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1993年學術文章
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name
X-linked mental retardation: in pursuit of a gene map.
@en
X-linked mental retardation: in pursuit of a gene map.
@nl
type
label
X-linked mental retardation: in pursuit of a gene map.
@en
X-linked mental retardation: in pursuit of a gene map.
@nl
prefLabel
X-linked mental retardation: in pursuit of a gene map.
@en
X-linked mental retardation: in pursuit of a gene map.
@nl
P2860
P1476
X-linked mental retardation: in pursuit of a gene map.
@en
P2093
Schwartz CE
P2860
P304
P407
P577
1993-06-01T00:00:00Z