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Prenatal Diagnosis of a Large Centromeric Heteromorphism of Chromosome 12: Implications for Genetic...

Prenatal Diagnosis of a Large Centromeric Heteromorphism of Chromosome 12: Implications for Genetic...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmed_primary_12576746

Prenatal Diagnosis of a Large Centromeric Heteromorphism of Chromosome 12: Implications for Genetic Counseling

About this item

Full title

Prenatal Diagnosis of a Large Centromeric Heteromorphism of Chromosome 12: Implications for Genetic Counseling

Publisher

Basel, Switzerland: Karger

Journal title

Fetal diagnosis and therapy, 2003-03, Vol.18 (2), p.111-113

Language

English

Formats

Publication information

Publisher

Basel, Switzerland: Karger

More information

Scope and Contents

Contents

Chromosomal centromeric variants can be found in the course of a prenatal diagnosis. When following the discovery of fetal abnormalities at ultrasound examination, such variants may lead to some difficulties in genetic counseling. Here we describe a new heteromorphism implicating chromosome 12, found in a fetus with a suspicion of microcephaly, and...

Alternative Titles

Full title

Prenatal Diagnosis of a Large Centromeric Heteromorphism of Chromosome 12: Implications for Genetic Counseling

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmed_primary_12576746

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmed_primary_12576746

Other Identifiers

ISSN

1015-3837

E-ISSN

1421-9964

DOI

10.1159/000068071

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