Schizencephaly in LEOPARD Syndrome-Reference-Cited by-同舟云学术

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Schizencephaly in LEOPARD Syndrome

Published:2009-07 Issue:1 Volume:41 Page:71-73
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Liang Jao-Shwann,Chien Yin-Hsiu,Hwu Wuh-Liang,Yeh Shu-Jen,Peng Shinn-Forng

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health

Reference16 articles.

1. Multiple lentigines syndrome;Gorlin;Am J Dis Child,1969

2. Multiple lentigines syndrome. Case report and review of the literature;Voron;Am J Med,1976

3. Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene;Digilio;Am J Hum Genet,2002

4. Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes;Sarkozy;J Med Genet,2003

5. PTPN11 mutations in patients with LEOPARD syndrome: A French multicentric experience;Keren;J Med Genet,2004

Cited by 4 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. RAF1-associated Noonan syndrome presenting antenatally with an abnormality of skull shape, subdural haematoma and associated with novel cerebral malformations;Clinical Dysmorphology;2017-04

2. Neuroimaging Findings in Pediatric Genetic Skeletal Disorders: A Review;Journal of Neuroimaging;2016-12-21

3. Freckles and Lentigines;The Melanocytic Proliferations;2014-01-17

4. LEOPARD Syndrome: Clinical Features and Gene Mutations;Molecular Syndromology;2012

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