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Microlissencephaly: a heterogeneous malformation of cortical development.Academic Article Why?
Dobyns, WilliamPerson Why?
Clinical and brain imaging heterogeneity of severe microcephaly.Academic Article Why?
Microcephaly, jejunal atresia, aberrant right bronchus, ocular anomalies, and XY sex reversal.Academic Article Why?
New recessive syndrome of microcephaly, cerebellar hypoplasia, and congenital heart conduction defect.Academic Article Why?
TALEN-based generation of a cynomolgus monkey disease model for human microcephaly.Academic Article Why?
The microcephaly-capillary malformation syndrome.Academic Article Why?
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations.Academic Article Why?
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis.Academic Article Why?
MCPH1 deletion in a newborn with severe microcephaly and premature chromosome condensation.Academic Article Why?
Microcephaly with simplified gyral pattern in six related children.Academic Article Why?
Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7q.Academic Article Why?
Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures.Academic Article Why?
Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly-capillary malformation syndrome.Academic Article Why?
Primary microcephaly: new approaches for an old disorder.Academic Article Why?
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