Chromosomal fragility and human genetic disorders.

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Chromosomal fragility and human genetic disorders.

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2000 nî lūn-bûn

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2000年の論文

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2000年学术文章

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2000年学术文章

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2000年学术文章

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2000年学术文章

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2000年学术文章

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2000年學術文章

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2000年學術文章

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2000年學術文章

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Chromosomal fragility and human genetic disorders.

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Chromosomal fragility and human genetic disorders.

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Item

label

Chromosomal fragility and human genetic disorders.

@ast

Chromosomal fragility and human genetic disorders.

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Chromosomal fragility and human genetic disorders.

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Chromosomal fragility and human genetic disorders.

@en

P1476

Chromosomal fragility and human genetic disorders.

@en

P2093

S Baskaran

http://www.w3.org/2001/XMLSchema#string

V Brahmachari

http://www.w3.org/2001/XMLSchema#string

P2860

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2

FMR1 protein: conserved RNP family domains and selective RNA binding

Simple tandem DNA repeats and human genetic disease

A marker X chromosome

FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: a new appraisal

Identification of the gene FMR2, associated with FRAXE mental retardation.

Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression

P2888

bf02867554

P304

145-157

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1007/BF02867554

http://www.w3.org/2001/XMLSchema#string

P433

Suppl 1

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2000-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

23105278

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P932

3454080

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