Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation-Reference-Cited by-同舟云学术

Genetic predisposition to fetal alcohol syndrome: association with congenital disorders of N-glycosylation

Published:2017-09-20 Issue:1 Volume:83 Page:119-127
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

de la Morena-Barrio María E,Ballesta-Martínez María J,López-Gálvez Raquel,Antón Ana I,López-González Vanessa,Martínez-Ribot Laia,Padilla José,Miñano Antonia,García-Algar Oscar,Del Campo Miguel,Corral Javier,Guillén-Navarro Encarna,Vicente Vicente

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://www.nature.com/articles/pr2017201.pdf

Reference32 articles.

1. Jalali GR, Vorstman JA, Errami A et al. Detailed analysis of 22q11.2 with a high density MLPA probe set. Hum Mutat 2008;29:433–440.

2. Hoyme HE, May PA, Kalberg WO et al. A practical clinical approach to diagnosis of fetal alcohol spectrum disorders: clarification of the 1996 institute of medicine criteria. Pediatrics 2005;115:39–47.

3. Hoyme HE, Kalberg WO, Elliott AJ et al. Updated clinical guidelines for diagnosing fetal alcohol spectrum disorders. Pediatrics 2016;138:e20154256.

4. Del Campo M, Jones KL . A review of the physical features of the fetal alcohol spectrum disorders. Eur J Med Genet 2016;60:55–64.

5. Jones KL, Smith DW . Recognition of the fetal alcohol syndrome in early infancy. Lancet 1973;302:999–1001.

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Analysis of Two Novel GPI Variants Disrupting H Bonds and Localization Characteristics of 55 Gene Variants Associated with Glucose-6-phosphate Isomerase Deficiency;Current Medical Science;2024-04

2. Post-translational modifications of histone and non-histone proteins in epigenetic regulation and translational applications in alcohol-associated liver disease: Challenges and research opportunities;Pharmacology & Therapeutics;2023-11

3. A Novel Compound Heterozygous Gene Mutation of Dolichol Kinase Deficiency (DOLK-CDG);Endocrine, Metabolic & Immune Disorders - Drug Targets;2023-02

4. Genetic Influences on Fetal Alcohol Spectrum Disorder;Genes;2023-01-12

5. Case Report: Identification of Two Variants of ALG13 in Families With or Without Seizure and Binocular Strabismus: Phenotypic Spectrum Analysis;Frontiers in Genetics;2022-07-11