Genetics of Microcephaly in Man
- 1 January 1959
- journal article
- research article
- Published by Cambridge University Press (CUP) in Acta geneticae medicae et gemellologiae
- Vol. 8 (1) , 75-86
- https://doi.org/10.1017/s1120962300019089
Abstract
SUMMARY According to recommendations in radiation and mutation genetics, made in 1956 at the Copenhagen Meeting of a study group of the World Health Organization, a registration of hereditary traits and clinical syndromes is being carried out within the District of Münster, Province of Westfalia (Germany) since 1957. One of the pathological conditions included in this research program is microcephaly investigated from a clinical as well as from a genetic stand-point. The preliminary results of our study on microcephaly in man are given in this report.Keywords
This publication has 4 references indexed in Scilit:
- Phenocopies and Genotype, with Special Reference to Sporadically-Occurring Developmental VariantsThe American Naturalist, 1957
- Some Problems in the Pathology of Mental Deficiency with MicrocephalyNeurology, 1956
- Microcephaly with Extensive Calcium Deposits and DemyelinationJournal of Neuropathology and Experimental Neurology, 1954
- Über diffuse symmetrische Kalkablagerungen bei einem Krankheitsbild mit Mikrocephalie und MeningoencephalitisArchiv Fur Psychiatrie Und Nervenkrankheiten, 1950