Karyotype, phenotype and parental origin in 19 cases of triploidy-Reference-Cited by-同舟云学术

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Karyotype, phenotype and parental origin in 19 cases of triploidy

Published:2001 Issue:12 Volume:21 Page:1034-1048
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Daniel Art,Wu Zhanhe,Bennetts Bruce,Slater Howard,Osborn Robert,Jackson Julianne,Pupko Vladimir,Nelson John,Watson Geoff,Cooke-Yarborough Claire,Loo Christine

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference26 articles.

1. Parental origin and mechanisms of formation of triploidy: a study of 25 cases

2. Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

3. Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child.

4. Morphologic anomalies in triploid liveborn fetuses

5. A diploid-triploid human mosaic with cytogenetic evidence of double fertilization

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3. Triploid pregnancy–Clinical implications;Clinical Genetics;2021-06

4. Distribution of diandric and digynic triploidy depending on gestational age;Journal of Assisted Reproduction and Genetics;2021-05-13

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