Prenatal diagnosis of a 5.44-Mb de novo 22q13.31q13.33 deletion encompassing SHANK3 associated with mosaicism for r(22)(p11.2q11.31) and monosomy 22 in a fetus with severe right hydronephrosis and hydroureter on ultrasound and determination of a mate

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Journal
Taiwanese Journal of Obstetrics and Gynecology
Published
2025-03-01
DOI
https://doi.org/10.1016/j.tjog.2024.12.011
Primary Topic
Genomic variations and chromosomal abnormalities
Type
article
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article

Prenatal diagnosis of a 5.44-Mb de novo 22q13.31q13.33 deletion encompassing SHANK3 associated with mosaicism for r(22)(p11.2q11.31) and monosomy 22 in a fetus with severe right hydronephrosis and hydroureter on ultrasound and determination of a mate

Peih-Shan Wu, Liang‐Kai Wang, Chih‐Ping Chen, Wayseen Wang et al.
Taiwanese Journal of Obstetrics and Gynecology
Genomic variations and chromosomal abnormalities
article

Prenatal diagnosis of a 5.44-Mb de novo 22q13.31q13.33 deletion encompassing SHANK3 associated with mosaicism for r(22)(p11.2q11.31) and monosomy 22 in a fetus with severe right hydronephrosis and hydroureter on ultrasound and determination of a mate

Peih-Shan Wu, Liang‐Kai Wang, Chih‐Ping Chen, Wayseen Wang, Fang-Tzu Wu, Yen-Ting Pan, Chen‐Wen Pan
article en

Abstract

No abstract available for this paper.
Taiwanese Journal of Obstetrics and GynecologyVol. 64(2)
China Medical University (TW), Mackay Memorial Hospital (TW), China Medical University Hospital (TW)
Zero hunger
Openalex Percentile: Top 95%
Genomic variations and chromosomal abnormalities
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