Prenatal sonographic features of triploidy at 12-16 weeks-Reference-Cited by-同舟云学术

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Prenatal sonographic features of triploidy at 12-16 weeks

Published:2016-07 Issue:7 Volume:36 Page:650-655
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Zalel Yaron¹,Shapiro Israel²,Weissmann-Brenner Alina¹,Berkenstadt Michal³,Leibovitz Zvi²,Bronshtein Moshe⁴

Affiliation:

1. Department of Obstetrics and Gynecology; The Chaim Sheba Medical Center; Tel-Hashomer Israel

2. Department of Obstetrics and Gynecology; Bnai-Zion Medical Center; Haifa Israel

3. Danek Gertner Institute of Human Genetic; The Chaim Sheba Medical Center; Tel-Hashomer Israel

4. Faculty of Social Welfare and Health Sciences; Haifa University; Haifa Israel

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference27 articles.

1. The origin of human triploids;Jacobs;Ann Hum Genet,1978

2. A cytogenetic study of 1000 spontaneous abortions;Hassold;Ann Hum Genet,1980

3. Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole;Zaragoza;Am J Hum Genet,2000

4. Maternal age and gestational age-specific risk for chromosomal defects;Snijders;Fetal Diagn Ther,1995

5. Prenatal diagnosis of chromosome abnormalities in the presence of fetal structural defects;Wladimiroff;Am J Med Genet,1988

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1. Ultrasound signs of fetal chromosomal abnormalities at 11–14 weeks of pregnancy and its value in the era of modern genetic testing;Ultrasound & Functional Diagnostics;2024-02-13

2. Overview of Noninvasive Prenatal Testing (NIPT) for the Detection of Fetal Chromosome Abnormalities; Differences in Laboratory Methods and Scope of Testing;Clinical Obstetrics & Gynecology;2023-07-17

3. Prenatal diagnosis of micrognathia: a systematic review;Frontiers in Pediatrics;2023-04-12

4. Non‐invasive prenatal screening for fetal triploidy using single nucleotide polymorphism‐based testing: Differential diagnosis and clinical management in cases showing an extra haplotype;Prenatal Diagnosis;2022-05-21

5. Prenatal diagnosis of syndromic alobar holoprosencephaly associated with digynic triploidy fetus;Romanian Journal of Morphology and Embryology;2021-06-25

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