The first report showing de novo partial 21q monosomy in an adult woman with occult primary ovarian insufficiency (POI)-Reference-Cited by-同舟云学术

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The first report showing de novo partial 21q monosomy in an adult woman with occult primary ovarian insufficiency (POI)

Published:2019-08-27 Issue:9 Volume:57 Page:e230-e233
ISSN:1437-4331
Container-title:Clinical Chemistry and Laboratory Medicine (CCLM)
language:
Short-container-title:

Author:

Zeng Jian,Huang Wujian,Huang Mingyan,Wang Zhihong

Funder

Natural Science Foundation of Fujian Province

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

https://www.degruyter.com/document/doi/10.1515/cclm-2018-1271/pdf

Reference20 articles.

1. Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature;Mol Cytogenet,2016

2. Genetics of primary ovarian insufficiency: a review;J Assist Reprod Genet,2014

3. A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing;Hum Mutat,2014

4. Genetics of primary ovarian insufficiency: a review;J Assist Reprod Genet,2014

5. Reliable and sensitive detection of fragile X (expanded) alleles in clinical prenatal DNA samples with a fast turnaround time;J Mol Diagn,2012

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1. A de novo pure 21q22.3 deletion in a 9-year-old boy with buried penis: a case report and literature review;Translational Pediatrics;2021-10

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