Clinical Genetics · 1983 · 26 citations · 10 references
Life SciencesGeneticsNeuroscienceHuman GeneticsMedical GeneticsNeurogeneticsGenetic DisordersInheritance PatternsMendelian DisordersMendelian InheritanceMendelian Neurological DisordersNeurogenetic DisordersAutosomal Dominant InheritanceCongenital MicrocephalyFamilial Inheritance PatternsMendelian Disorder GeneticsMendelian Neurodevelopmental DisordersMicrocephaly MutationsPediatric Neurogenetic Disorders
Thirteen patients from three unrelated families were found to have microcephaly, without any neurological or dysmorphic manifestations. Autosomal dominant inheritance is concluded since the trait was transmitted directly in all three families, including one male-to-male instance. The recognition of this uncomplicated form of microcephaly as a Mendelian trait further extends its etiological heterogeneity.
10
Kenneth Lyons Jones, David W. Smith · Teratology · 1975 · 450 citations
Annals of Internal Medicine · 1979 · 421 citations · Full text
Intra-uterine Methylmercury Poisoning in Iraq
Laman Amin‐Zaki, Sami B. Elhassani, Mohamed A. Majeed et al. · PEDIATRICS · 1974 · 318 citations
Congenital and Maternal Toxoplasmosis
J Couvreur, G Desmonts · Developmental Medicine & Child Neurology · 1962 · 128 citations
Medicine, Pathology, Pediatrics +14