Genetic components of perinatal morbidity and mortality. - Wikidata - wikimedia - TriplyDB

Genetic components of perinatal morbidity and mortality.

Genetic components of perinatal morbidity and mortality.

http://www.wikidata.org/entity/Q34305385

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Genetic components of perinatal morbidity and mortality.

http://www.wikidata.org/entity/Q34305385

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2001 nî lūn-bûn

@nan

2001 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2001年の論文

@ja

2001年論文

@yue

2001年論文

@zh-hant

2001年論文

@zh-hk

2001年論文

@zh-mo

2001年論文

@zh-tw

2001年论文

@wuu

name

Genetic components of perinatal morbidity and mortality.

@ast

Genetic components of perinatal morbidity and mortality.

@en

Genetic components of perinatal morbidity and mortality.

@nl

type

label

Genetic components of perinatal morbidity and mortality.

@ast

Genetic components of perinatal morbidity and mortality.

@en

Genetic components of perinatal morbidity and mortality.

@nl

prefLabel

Genetic components of perinatal morbidity and mortality.

@ast

Genetic components of perinatal morbidity and mortality.

@en

Genetic components of perinatal morbidity and mortality.

@nl

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Journal of Perinatal Medicine

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Genetic components of perinatal morbidity and mortality.

@en

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Beke A

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Papp Z

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P2860

Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis.

Albright's hereditary osteodystrophy: a review

Incontinentia pigmenti (Bloch-Sulzberger syndrome).

Syndromic association of cleft palate, bilateral choanal atresia, curly hair, and congenital hypothyroidism.

Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft für Pädiatrische Nephrologie

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.

The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3.

Molecular epidemiology of familial hypercholesterolaemia.

Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.

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230-234

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scholarly article

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10.1515/JPM.2001.032

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3

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29

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2001-01-01T00:00:00Z

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11447927

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