Microcephaly in the Netherlands: a clinical and genetical study.
about
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pterAutosomal Recessive Primary Microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuumAutosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findingsFamilial bird-headed dwarfism (Seckel's syndrome).Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32Apparent microcephaly caused by a bicornuate uterus.Molecular genetics of human primary microcephaly: an overview.A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family.Protein-truncating mutations in ASPM cause variable reduction in brain size.Microcephaly with simplified gyral pattern in six related children.Autosomal recessive microcephaly with neonatal myoclonic seizures: clinical and MRI findings.Recessive (true) microcephaly: a case report with neuropathological observations.Primary autosomal recessive microcephaly: homozygosity mapping of MCPH4 to chromosome 15.Chronic illness in preschool Jordanian children.Autosomal recessive primary microcephaly due to ASPM mutations: An update.
P2860
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P2860
Microcephaly in the Netherlands: a clinical and genetical study.
description
1959 nî lūn-bûn
@nan
1959年の論文
@ja
1959年論文
@yue
1959年論文
@zh-hant
1959年論文
@zh-hk
1959年論文
@zh-mo
1959年論文
@zh-tw
1959年论文
@wuu
1959年论文
@zh
1959年论文
@zh-cn
name
Microcephaly in the Netherlands: a clinical and genetical study.
@en
type
label
Microcephaly in the Netherlands: a clinical and genetical study.
@en
prefLabel
Microcephaly in the Netherlands: a clinical and genetical study.
@en
P1476
Microcephaly in the Netherlands: a clinical and genetical study.
@en
P2093
VAN DEN BOSCH J
P304
P356
10.1111/J.1469-1809.1958.TB01455.X
P407
P577
1959-04-01T00:00:00Z