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Humangenetik|January 1, 1975
Heterozygote tests and genetic counseling in maple syrup urine disease: an application of Baye's theoremU Langenbeck, T Grimm, H W Rüdiger, et al.
Humangenetik|May 26, 1975
A 46,XX,10Q+ chromosome constitution in a girl. Partial long arm duplication or insertional translocation?E Orye, H Verhaaren, K Samuël, et al.
Humangenetik|May 26, 1975
The diagnosis of the early infantile form of hypophosphatasia tardaJ Svejcar, A Walther
Humangenetik|June 19, 1975
[Phenotypic variation in partial trisomy 4q (author's transl)]W Vogel, J W Siebers, J Gunkel
Humangenetik|June 19, 1975
G-6-PD Poznań, variant with severe enzyme deficiencyA L Pawlak, C A Mazurkiewicz, J Ordyński, et al.
Humangenetik|July 23, 1975
[Familial neuroblastoma: cytogenetic investigation of the peripheral blood (author's transl)]H Klein, E Plöchl, F Lampert
Humangenetik|December 23, 1975
[Various banding simultaneously obtained on the same slides, after treatment by BrdU (author's transl)]Dutrillaux
Humangenetik|September 23, 1975
Chromosomal damage in chronic alcohol usersG Obe, J Herha
Humangenetik|September 23, 1975
Prenatal diagnosis of trisomy 9U Francke, K Benirschke, O W Jones
Humangenetik|August 25, 1975
Three chromosome abnormalities (trisomy 21, XXY, and a de nova reciprocal translocation) in a child with 48, XXY, + 21,T(6;10)(P22-24;P12)P D Buchanan
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