Prenatal diagnosis of 13q- syndrome in a fetus with holoprosencephaly and thumb agenesis-Reference-Cited by-同舟云学术

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Prenatal diagnosis of 13q- syndrome in a fetus with holoprosencephaly and thumb agenesis

Published:2001-02 Issue:2 Volume:17 Page:166-168
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics and Gynecology
language:en
Short-container-title:Ultrasound Obstet Gynecol

Author:

Gutierrez J.,Sepulveda W.,Saez R.,Carstens E.,Sanchez J.

Publisher

Wiley

Subject

Obstetrics and Gynaecology,Radiology Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Reference8 articles.

1. 1 KL Jones . Smith's Recognizable Patterns of Human Malformation , 5th edn . Philadelphia: W.B. Saunders, 1997 : 60, 1

2. Chromosome deletion in a case of retinoblastoma

3. Preliminary definition of a “critical region” of chromosome 13 in q32: Report of 14 cases with 13q deletions and review of the literature

4. PRENATAL DIAGNOSIS OF PARTIAL MONOSOMY 13q ASSOCIATED WITH OCCIPITAL ENCEPHALOCOELE IN A FETUS

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2. From Genes to Ambiguity: A Case Study Exploring the Enigmatic Connection Between Chromosome 13q Deletion Syndrome and Ambiguous Genitalia;Cureus;2023-09-13

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4. A case of prenatally diagnosed partial monosomy 13q syndrome;Cukurova Medical Journal (Çukurova Üniversitesi Tıp Fakültesi Dergisi);2017-03-31

5. Prenatal Detection and Postnatal Follow-Up of Segmental Aneusomies of Chromosome 13 in 4 Consecutive Pregnancies in an Ethnic South Indian Family With a Maternally Inherited Balanced Translocation;Laboratory Medicine;2015-11-01

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