Prenatal diagnosis ofde novo pure partial monosomy 4p (4p15.1 ? pter) in a growth-restricted fetus with a Greek warrior helmet face and unilateral facial cleft on three-dimensional ultrasound-Reference-Cited by-同舟云学术

Prenatal diagnosis ofde novo pure partial monosomy 4p (4p15.1 ? pter) in a growth-restricted fetus with a Greek warrior helmet face and unilateral facial cleft on three-dimensional ultrasound

Published:2004 Issue:11 Volume:24 Page:934-936
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Chen Chih-Ping,Hsu Chin-Yuan,Lee Chen-Chi,Chen Wen-Lin,Chen Li-Feng,Wang Wayseen

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference12 articles.

1. Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity

2. Prenatal recognition of 4p- syndrome.

3. Prenatal diagnosis of brain abnormalities in Wolf-Hirschhorn (4p-) syndrome

4. Clinical, Cytogenetic and Molecular Investigation in a Fetus with Wolf-Hirschhorn Syndrome with Paternally Derived 4p Deletion

5. Partial deletion of 4p in fetal cells not present in chorionic villi

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1. Wolf–Hirschhorn syndrome: Prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1 → pter) in a fetus with facial cleft and preaxial polydactyly;Taiwanese Journal of Obstetrics and Gynecology;2020-05

2. Prenatal diagnosis of Wolf-Hirschhorn syndrome: Ultrasonography and molecular karyotyping results;European Journal of Obstetrics & Gynecology and Reproductive Biology;2018-06

3. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones;Taiwanese Journal of Obstetrics and Gynecology;2017-12

4. Réponse à l’article de F. Vialard et al. : la prévalence des microdélétions et microduplications pathogènes récurrentes en diagnostic prénatal doit-elle amener à revoir l’évolution des techniques de dépistage non invasif ? L’exemple de la région 22q11.2;Gynécologie Obstétrique Fertilité & Sénologie ;2017-01

5. Chromosomal deletions detected at amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2014-03