Growth hormone deficiency, aortic dilation, and neurocognitive issues in Feingold syndrome 2-Reference-Cited by-同舟云学术

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Growth hormone deficiency, aortic dilation, and neurocognitive issues in Feingold syndrome 2

Published:2019-01-23 Issue:3 Volume:179 Page:410-416
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Muriello Michael¹²^ORCID,Kim Alexander Y.¹,Sondergaard Schatz Krista¹,Beck Natalie¹³,Gunay‐Aygun Meral¹,Hoover‐Fong Julie E.¹³^ORCID

Affiliation:

1. McKusick‐Nathans Institute of Genetic MedicineJohns Hopkins University Baltimore Maryland

2. Department of PediatricsMedical College of Wisconsin Milwaukee Wisconsin

3. Greenberg Center for Skeletal DysplasiaJohns Hopkins University Baltimore Maryland

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61037

Reference20 articles.

1. Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31.1-13q32.3

2. Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans

3. Neurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2

4. Expanding the phenotype of feingold syndrome-2

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1. Multivessel Coronary Artery Dissection in a Patient with Co-Occurrence of Aortic Dissection and Dilated Cardiomyopathy in the Postpartum Period;Diseases;2023-12-10

2. SARS-CoV-2 airway infection results in the development of somatosensory abnormalities in a hamster model;Science Signaling;2023-05-09

3. Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing;Frontiers in Endocrinology;2022-09-27

4. SARS-CoV-2 Airway Infection Results in Time-dependent Sensory Abnormalities in a Hamster Model;2022-08-19

5. First Patient Diagnosed as Feingold Syndrome Type 2 with Alport Syndrome and Review of the Current Literature;Molecular Syndromology;2022

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