Central 22q11.2 deletion ( LCR22 B‐D ) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Central 22q11.2 deletion ( LCR22 B‐D ) in a fetus with severe fetal growth restriction and a mother with severe systemic lupus erythematosus: Further evidence of CRKL haploinsufficiency in the pathogenesis of 22q11.2 deletion syndrome

Published:2021-07 Issue:10 Volume:185 Page:3042-3047
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Lin Isabella¹,Afshar Yalda¹²,Goldstein Jeffrey³,Grossman Jennifer¹⁴,Grody Wayne W.¹³⁵,Quintero‐Rivera Fabiola⁶

Affiliation:

1. David Geffen School of Medicine University of California Los Angeles Los Angeles California USA

2. Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology University of California Los Angeles Los Angeles California USA

3. Pathology and Laboratory Medicine UCLA Center for Health Sciences Los Angeles California USA

4. Division of Rheumatology, Department of Medicine University of California Los Angeles California USA

5. Department of Human Genetics University of California Los Angeles Los Angeles California USA

6. Departments of Pathology and Laboratory Medicine and Pediatrics, Division of Genetic and Genomic Medicine University of California Irvine California USA

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62346

Reference23 articles.

1. Emerging Treatment Models in Rheumatology: Antiphospholipid Syndrome and Pregnancy: Pathogenesis to Translation

2. CHORANGIOMA AND RELATED VASCULAR LESIONS OF THE PLACENTA — A REVIEW

3. 22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features

4. Prenatal Sonographic Features of 22q11.2 Microdeletion Syndrome

5. Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

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4. Frequency of chromosome 22q11.2 deletion among newborns with non-syndromic congenital heart defects from western Mexico;Boletín Médico del Hospital Infantil de México;2022-11-09

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