Prenatal phenotype of 47, XXY (Klinefelter syndrome)-Reference-Cited by-同舟云学术

Prenatal phenotype of 47, XXY (Klinefelter syndrome)

Published:2021-12-07 Issue: Volume: Page:
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Swanson Kate¹²^ORCID,Bishop Juliet C.³⁴,Al‐Kouatly Huda B.⁵^ORCID,Makhamreh Mona⁵,Felton Thomas⁶,Vora Neeta L.⁷^ORCID,Sparks Teresa N.¹^ORCID,Jelin Angie C.³⁴^ORCID

Affiliation:

1. Division of Maternal‐Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences University of California San Francisco California USA

2. Division of Medical Genetics, Department of Pediatrics University of California San Francisco California USA

3. Division of Maternal‐Fetal Medicine, Department of Gynecology and Obstetrics The Johns Hopkins University School of Medicine Baltimore Maryland USA

4. Department of Genetic Medicine The Johns Hopkins University School of Medicine Baltimore Maryland USA

5. Division of Maternal‐Fetal Medicine Sidney Kimmel Medical College of Thomas Jefferson University Philadelphia Pennsylvania USA

6. McLendon Clinical Laboratories, Cytogenetics Laboratory University of North Carolina Health Chapel Hill North Carolina USA

7. Division of Maternal‐Fetal Medicine, Department of Obstetrics and Gynecology University of North Carolina at Chapel Hill School of Medicine Chapel Hill North Carolina USA

Funder

Fetal Health Foundation

National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6071

Reference16 articles.

1. Prenatal and Postnatal Prevalence of Klinefelter Syndrome: A National Registry Study

2. Klinefelter's syndrome