A case of partial paternal uniparental isodisomy of chromosome 7 with no phenotypic abnormalities
Saved in:
Main Authors: | Fangfang liu, Zhao Wang, Xiaoyi Wang, Dengju Xie |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2025-01-01
|
Series: | Taiwanese Journal of Obstetrics & Gynecology |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1028455924003024 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A Korean Patient With Leber Congenital Amaurosis and a Homozygous RPE65 Variant Originating From a Paternal Uniparental Isodisomy
by: Hane Lee, et al.
Published: (2025-01-01) -
Uniparental maternal tetrasomy X co-occurrence with paternal nondisjunction: investigation of the origin of 48,XXXX
by: Keiko Shimojima Yamamoto, et al.
Published: (2024-08-01) -
Prenatal diagnosis and genetic counselling of a rare maternal inherited chromosome 1q21.1q21.2 microduplication with no phenotypic abnormalities
by: Mingxia Xie, et al.
Published: (2025-01-01) -
HB H DISEASE CAUSED BY UNIPARENTAL DISOMY: FIRST REPORT OF THE αT-SAUDIΑ MUTATION IN THE CHINESE POPULATION
by: Ge Wang, et al.
Published: (2024-08-01) -
Down-Turner Syndrome: A Case with Double Monoclonal Chromosomal Abnormality
by: Gioconda Manassero-Morales, et al.
Published: (2016-01-01)