Molecular cytogenetic diagnosis of Williams syndrome.

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Single signal of the Williams syndrome chromosome region 1 gene in hyperploidic bone marrow cells of acute lymphoblastic leukemia in a Williams syndrome patient.

P2860

Q52124111-9BC5698A-1AA0-42C4-A09C-170F4D66607A

P2860

Molecular cytogenetic diagnosis of Williams syndrome.

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http://www.wikidata.org/entity/Q52008067

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1996 nî lūn-bûn

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1996年の論文

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1996年学术文章

@wuu

1996年学术文章

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1996年学术文章

@zh-cn

1996年学术文章

@zh-hans

1996年学术文章

@zh-my

1996年学术文章

@zh-sg

1996年學術文章

@yue

1996年學術文章

@zh-hant

name

Molecular cytogenetic diagnosis of Williams syndrome.

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Molecular cytogenetic diagnosis of Williams syndrome.

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type

Item

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Molecular cytogenetic diagnosis of Williams syndrome.

@en

Molecular cytogenetic diagnosis of Williams syndrome.

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Molecular cytogenetic diagnosis of Williams syndrome.

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Molecular cytogenetic diagnosis of Williams syndrome.

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P1476

Molecular cytogenetic diagnosis of Williams syndrome.

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P2093

Ando M

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Hirota H

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Imamura S

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Joh-o K

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Kimura M

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Matsuoka R

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Momma K

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Takao A

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P2860

Human smooth muscle myosin heavy chain gene mapped to chromosomal region 16q12

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene.

Natural history of Williams syndrome: physical characteristics.

Spectrum of findings in a family with nonsyndromic autosomal dominant supravalvular aortic stenosis: a Doppler echocardiographic study.

The Williams elfin facies syndrome. A new perspective.

The elfin facies syndrome.

Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.

Elastin and vascular disease.

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

P304

473-477

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scholarly article

P356

10.1002/(SICI)1096-8628(19960823)64:3<473::AID-AJMG5>3.0.CO;2-Q

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P433

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P478

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1996-08-01T00:00:00Z

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P698

8862624

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Molecular cytogenetic diagnosis of Williams syndrome.

about

P2860

P2860

Molecular cytogenetic diagnosis of Williams syndrome.

description

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698