Investigation of genetic causes of intellectual disability in kerman province, South East of iran.

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Investigation of genetic causes of intellectual disability in kerman province, South East of iran.

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2012 nî lūn-bûn

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2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

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name

Investigation of genetic cause ...... province, South East of iran.

@ast

Investigation of genetic cause ...... province, South East of iran.

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type

Item

label

Investigation of genetic cause ...... province, South East of iran.

@ast

Investigation of genetic cause ...... province, South East of iran.

@en

prefLabel

Investigation of genetic cause ...... province, South East of iran.

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Investigation of genetic cause ...... province, South East of iran.

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P1476

Investigation of genetic cause ...... province, South East of iran.

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P2093

E Jafari

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F Behjati

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F Sabbagh

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Gh R Kavoosi

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H Darvish

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H Najmabadi

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I Bahman

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K Kahrizi

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M J Soltani Banavandi

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M Mohseni

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P2860

Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter

A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation

Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity

Primer3 on the WWW for general users and for biologist programmers

A simple salting out procedure for extracting DNA from human nucleated cells

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings

X-linked mental retardation (XLMR): from clinical conditions to cloned genes.

Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation

Use of tandem mass spectrometry for multianalyte screening of dried blood specimens from newborns.

P304

79-85

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scholarly article

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2012-02-01T00:00:00Z

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22737560

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P921

disability

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3372047

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