NCAPH

Panel	Reviews	Mode of inheritance	Details
Red NCAPH in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Microcephaly 23, primary, autosomal recessive 617985
Red NCAPH in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.269	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Microcephaly 23, primary, autosomal recessive 617985

Panel

Reviews

Mode of inheritance

Details

Version 1.1902

review

BIALLELIC, autosomal or pseudoautosomal

Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review

BIALLELIC, autosomal or pseudoautosomal

2 panels