Frontotemporal pachygyria-Two new patients

Kristiina Avela; Sanna-Maria Toiviainen-Salo; Pirkko Karttunen-Lewandowski; Leena Kauria; Leena Valanne; Riitta Salonen-Kajander

doi:10.1016/j.ejmg.2012.09.007

Frontotemporal pachygyria-Two new patients

Kristiina Avela, Sanna-Maria Toiviainen-Salo, Pirkko Karttunen-Lewandowski, Leena Kauria, Leena Valanne, Riitta Salonen-Kajander

Research output: Contribution to journal › Article › Scientific › peer-review

Original language	English
Journal	European Journal of Medical Genetics
Volume	55
Issue number	12
Pages (from-to)	753-757
Number of pages	5
ISSN	1769-7212
DOIs	https://doi.org/10.1016/j.ejmg.2012.09.007
Publication status	Published - Dec 2012
MoE publication type	A1 Journal article-refereed

Fields of Science

Lissencephaly
Pachygyria
Simplified gyral pattern
Brain malformation
Mental retardation
NEURONAL MIGRATION
CEREBELLAR HYPOPLASIA
MUTATIONS
DISORDER
3111 Biomedicine

Access to Document

10.1016/j.ejmg.2012.09.007

Cite this

@article{a736471747fc4f5a9d7b9dd8c1009283,

title = "Frontotemporal pachygyria-Two new patients",

keywords = "Lissencephaly, Pachygyria, Simplified gyral pattern, Brain malformation, Mental retardation, NEURONAL MIGRATION, CEREBELLAR HYPOPLASIA, MUTATIONS, DISORDER, 3111 Biomedicine",

author = "Kristiina Avela and Sanna-Maria Toiviainen-Salo and Pirkko Karttunen-Lewandowski and Leena Kauria and Leena Valanne and Riitta Salonen-Kajander",

year = "2012",

month = dec,

doi = "10.1016/j.ejmg.2012.09.007",

language = "English",

volume = "55",

pages = "753--757",

journal = "European Journal of Medical Genetics",

issn = "1769-7212",

publisher = "Elsevier Scientific Publ. Co",

number = "12",

}

TY - JOUR

T1 - Frontotemporal pachygyria-Two new patients

AU - Avela, Kristiina

AU - Toiviainen-Salo, Sanna-Maria

AU - Karttunen-Lewandowski, Pirkko

AU - Kauria, Leena

AU - Valanne, Leena

AU - Salonen-Kajander, Riitta

PY - 2012/12

Y1 - 2012/12

KW - Lissencephaly

KW - Pachygyria

KW - Simplified gyral pattern

KW - Brain malformation

KW - Mental retardation

KW - NEURONAL MIGRATION

KW - CEREBELLAR HYPOPLASIA

KW - MUTATIONS

KW - DISORDER

KW - 3111 Biomedicine

U2 - 10.1016/j.ejmg.2012.09.007

DO - 10.1016/j.ejmg.2012.09.007

M3 - Article

SN - 1769-7212

VL - 55

SP - 753

EP - 757

JO - European Journal of Medical Genetics

JF - European Journal of Medical Genetics

IS - 12

ER -