Home LiteratureArticle Details

PMID: 1710601 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death.

Genomics ·Vol. 10 ·No. 1 ·1991-05-00 ·Pages 298-9

Ivaschenko TE, White MB, Dean M, Baranov VS

Abstract

暂无摘要

Related Genes

CFTR

MeSH Terms

Chromosome Deletion Cystic Fibrosis/diagnosis,ethnology,genetics,mortality Cystic Fibrosis Transmembrane Conductance Regulator Exons Female Humans Infant, Newborn Male Membrane Proteins/genetics Pedigree Polymerase Chain Reaction Prenatal Diagnosis USSR

Chemicals

CFTR protein, human Membrane Proteins Cystic Fibrosis Transmembrane Conductance Regulator

Authors & Affiliations

4 authors, click to expand affiliations / ORCID

Ivaschenko T E

Laboratory of Prenatal Diagnosis of Inherited Diseases, All-Union Center for Prenatal Diagnosis of Cystic Fibrosis, Leningrad, USSR.

White M B

Dean M

Baranov V S

Article Info

Journal

Genomics

Abbr.

Genomics

ISSN

0888-7543

DOI

10.1016/0888-7543(91)90517-i

Published

1991-05-00

Pages

298-9

Language

English

Region

United States

NLM ID

8800135

Subset

Grants

NCI NIH HHS · N01-CO-74102 · United States

External Links

PubMed source DOI: 10.1016/0888-7543(91)90517-i View journal details

Analysis Services

A deletion of two nucleotides in exon 10 of the CFTR gene in a Soviet family with cystic fibrosis causing early infant death.

Contact

WeChat Official Account