European journal of human genetics : EJHG

Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.

Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.

Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor.

Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor.

Enrichment of HapMap recombination hotspot predictions around human nervous system genes: evidence for positive selection?

Enrichment of HapMap recombination hotspot predictions around human nervous system genes: evidence for positive selection?

Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.

Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.

Evolutionary genetics: the human brain -- adaptation at many levels.

Evolutionary genetics: the human brain -- adaptation at many levels.