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PMID: 2858726 Published · ppublish English Letter

Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome.

Lancet (London, England) ·Vol. 1 ·No. 8433 ·1985-04-13 ·Pages 871

Oberlé I, Mandel JL, Boué J, Mattei MG, Mattei JF

Abstract

暂无摘要

MeSH Terms
Chorionic Villi DNA/genetics Factor IX/genetics Female Fetal Diseases/diagnosis,genetics Fragile X Syndrome/diagnosis,genetics Genetic Markers Humans Male Pedigree Polymorphism, Genetic Pregnancy Prenatal Diagnosis Sex Chromosome Aberrations/diagnosis
Chemicals
Genetic Markers Factor IX DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Oberlé I
Mandel J L
Boué J
Mattei M G
Mattei J F
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
0140-6736
DOI
10.1016/s0140-6736(85)92228-7
Published
1985-04-13
Pages
871
Language
English
Region
England
NLM ID
2985213R
Subset
IM
External Links
PubMed source DOI: 10.1016/s0140-6736(85)92228-7 View journal details
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