Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: An inherited encephalopathy of childhood?-Reference-Cited by-同舟云学术

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Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: An inherited encephalopathy of childhood?

Published:2001 Issue:3 Volume:103 Page:198-206
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Nokelainen Pekka,Heiskala Hannu,Raininko Raili,Autti Taina,Wirtavuori Kari,H�kkinen Anna-Maija,Flint Jonathan

Publisher

Wiley

Subject

Genetics(clinical)

Reference26 articles.

1. Magnetic resonance techniques in neuronal ceroid lipofuscinoses and some other lysosomai diseases affecting the brain

2. Examination of the X chromosome by STS-PCR screening for the presence of submicroscopic deletions

3. An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformation

4. Aetiological findings and associated factors in children with severe mental retardation

Cited by 1 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. L;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

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