Variability of non‐lethal Fowler syndrome phenotype associated with FLVCR2 variants-Reference-Cited by-同舟云学术

Variability of non‐lethal Fowler syndrome phenotype associated with FLVCR2 variants

Published:2020-09-09 Issue:5 Volume:98 Page:520-521
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Al‐Murshedi Fathiya¹²,Mirza Hassan³,Al‐Saegh Abeer¹²,Al‐Nabhani Maryam¹,Al‐Shabibi Saud⁴,Baawain Saleh⁵,Al‐Futaisi Amna⁶,Al‐Shehhi Wafaa⁷,Al‐Maawali Almundher¹²^ORCID

Affiliation:

1. Department of Genetics, College of Medicine and Health Sciences Sultan Qaboos University Muscat Oman

2. Genetic and Developmental Medicine Clinic Sultan Qaboos University Hospital Muscat Oman

3. Department of Behavioral Medicine Sultan Qaboos University Hospital Muscat Oman

4. Department of Radiology, Royal Hospital Ministry of Health Muscat Oman

5. Department of Radiology and Molecular Imaging Sultan Qaboos University Hospital Muscat Oman

6. Department of Child Health, College of Medicine and Health Sciences Sultan Qaboos University Muscat Oman

7. Department of Pediatrics Royal Hospital, Ministry of Health Muscat Oman

Funder

Sultan Qaboos University

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13838

Reference4 articles.

1. Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): Report of 16 fetal cases

2. Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome)

3. Expanding the clinical spectrum of fowler syndrome: three siblings with survival into adulthood and systematic review of the literature;De Luca C;Clin Genet,2020

4. Mutations in FLVCR2 associated with Fowler syndrome and survival beyond infancy

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