Cytogenetic analysis in prenatal diagnosis. - Wikidata - awgldk - TriplyDB

Cytogenetic analysis in prenatal diagnosis.

Cytogenetic analysis in prenatal diagnosis.

http://www.wikidata.org/entity/Q33581918

about

Application of Neural Networks for classification of Patau, Edwards, Down, Turner and Klinefelter Syndrome based on first trimester maternal serum screening data, ultrasonographic findings and patient demographics.

P2860

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P2860

Cytogenetic analysis in prenatal diagnosis.

http://www.wikidata.org/entity/Q33581918

description

1993 nî lūn-bûn

@nan

1993 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

1993 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

1993年の論文

@ja

1993年論文

@yue

1993年論文

@zh-hant

1993年論文

@zh-hk

1993年論文

@zh-mo

1993年論文

@zh-tw

1993年论文

@wuu

name

Cytogenetic analysis in prenatal diagnosis.

@ast

Cytogenetic analysis in prenatal diagnosis.

@en

Cytogenetic analysis in prenatal diagnosis.

@nl

type

label

Cytogenetic analysis in prenatal diagnosis.

@ast

Cytogenetic analysis in prenatal diagnosis.

@en

Cytogenetic analysis in prenatal diagnosis.

@nl

prefLabel

Cytogenetic analysis in prenatal diagnosis.

@ast

Cytogenetic analysis in prenatal diagnosis.

@en

Cytogenetic analysis in prenatal diagnosis.

@nl

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P2860

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P1433

Western Journal of Medicine

P1476

Cytogenetic analysis in prenatal diagnosis

@en

P2093

Schonberg SA

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

P2860

Chromosomal mosaicism confined to the placenta in human conceptions

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies.

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.

Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes.

The phenotype of 45,X/46,XY mosaicism: an analysis of 92 prenatally diagnosed cases.

A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes.

Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens

Uniparental disomy for chromosome 16 in humans.

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy

P304

360-365

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scholarly article

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P433

3

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P478

159

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P577

1993-09-01T00:00:00Z

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8236978

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P932

1011351

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