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Human Genetics|November 1, 1979
Partial trisomy 13q21toqter de novo due to a recombinant chromosome rec(13)dup qM HabedankHumangenetik|September 23, 1975
Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced stateM Habedank, G KampeHuman Genetics|June 27, 1978
Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11)M Habedank, J FaustJournal of Medical Genetics|October 1, 1983
Monosomy 18p and pure trisomy 18p in a family with translocation (7;18)M Habedank, G Trost-BrinkhuesEuropean Journal of Pediatrics|August 16, 1976
The 18 p-syndrome. Report of four casesJ Faust, M Habedank, C NieuwenhuijsenHuman Genetics|May 19, 1976
GD (--) Aachen, a new variant of deficient glucose-6-phosphate dehydrogenase. Clinical, genetic, biochemical aspectsA Kahn, A Esters, M HabedankMutation Research|August 1, 1993
Effect of human and recombinant IFN-alpha and IFN-beta on the sister-chromatid exchange (SCE) frequency in amniotic fluid cells in vitroR Mertens, K Severin, M HabedankEuropean Journal of Pediatrics|August 17, 1978
Cranial morphology in the 18p-syndromeJ Faust, F Kotlarek, M HabedankKlinische Padiatrie|July 1, 1985
[Increased rate of sister chromatid exchange following therapy of acute lymphoblastic leukemias and non-Hodgkin lymphomas in childhood]R Mertens, B Weidmann, M HabedankZeitschrift Fur Geburtshilfe Und Perinatologie|December 1, 1980
[Prenatal diagnosis of trisomy 18 via hydramnion detected by echosonography (author's transl)]A Schotten, K J Esser, M HabedankPageof 6