The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
about
Mutations in SLC34A2 cause pulmonary alveolar microlithiasis and are possibly associated with testicular microlithiasisA developmental and genetic classification for malformations of cortical development: update 2012Emerging roles of Axin in cerebral cortical developmentRibosomal protein gene knockdown causes developmental defects in zebrafish.Is the novel SCKL3 at 14q23 the predominant Seckel locus?Kinetochore Malfunction in Human Pathologies.Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly.Severe form of Cockayne syndrome with varying clinical presentation and no photosensitivity in a family.Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways.
P2860
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P2860
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
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2000 nî lūn-bûn
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The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
@ast
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
@en
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
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label
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
@ast
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
@en
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
@nl
prefLabel
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
@ast
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
@en
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
@nl
P2093
P2860
P356
P1476
The novel genetic disorder microhydranencephaly maps to chromosome 16p13.3-12.1.
@en
P2093
P2860
P304
P356
10.1086/302898
P407
P577
2000-04-04T00:00:00Z