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Prenatal screening of cytogenetic anomalies - a Western Indian experience

Prenatal screening of cytogenetic anomalies - a Western Indian experience

http://www.wikidata.org/entity/Q35413270

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Cytogenetic analysis in couples with recurrent miscarriages: a retrospective study from Punjab, north India.Why do patients decline amniocentesis? Analysis of factors influencing the decision to refuse invasive prenatal testing.

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Prenatal screening of cytogenetic anomalies - a Western Indian experience

http://www.wikidata.org/entity/Q35413270

description

2015 nî lūn-bûn

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2015 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2015年の論文

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2015年論文

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2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

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2015年论文

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name

Prenatal screening of cytogenetic anomalies - a Western Indian experience

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Prenatal screening of cytogenetic anomalies - a Western Indian experience

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Prenatal screening of cytogenetic anomalies - a Western Indian experience

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Prenatal screening of cytogenetic anomalies - a Western Indian experience

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Prenatal screening of cytogenetic anomalies - a Western Indian experience

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Prenatal screening of cytogenetic anomalies - a Western Indian experience

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BMC Pregnancy and Childbirth

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Prenatal screening of cytogenetic anomalies - a Western Indian experience

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Bhumika Patel

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Chirag Modi

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Frenny Sheth

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Jayesh Sheth

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Manisha Desai

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Mizanur Rahman

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Sunil Trivedi

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Thomas Liehr

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P2860

Amniocentesis and chorionic villus sampling for prenatal diagnosis

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding

Frequency of births with potentially avoidable serious chromosomal anomalies in EEC countries, 1979-1982.

Inherited structural cytogenetic abnormalities detected incidentally in fetuses diagnosed prenatally: frequency, parental-age associations, sex-ratio trends, and comparisons with rates of mutants

Genetic disorders in children and young adults: a population study.

Enrichment, immunomorphological, and genetic characterization of fetal cells circulating in maternal blood

Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.

The prevalence of congenital anomalies in Europe.

The European Perinatal Health Report: comparing the health and care of pregnant women and newborn babies in Europe.

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