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Zeitschrift Fur Kinder- Und Jugendpsychiatrie|June 1, 1994
[Sex chromosome aberration with the 48 XYYY karyotype. A case report of the phenotype of a rare sex chromosome aneuploidy]A Stein, H Heilbronner, J JungmannDeutsche Medizinische Wochenschrift (1946)|May 15, 1981
[Prenatal diagnosis of Gaucher's disease (author's transl)]H Heilbronner, K G Wurster, K HarzerChromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 2, 2001
Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs)H Kühl, S Röttger, H Heilbronner, et al.Archives of Toxicology|June 16, 1978
[Chromosome studies on trichloroethylene workers (author's transl)]H Konietzko, W Haberlandt, H Heilbronner, et al.Journal of Cancer Research and Clinical Oncology|January 1, 1983
In vivo induction of neoplastic growth in nude mouse connective tissue adjacent to xenografted human tumorsH J Staab, H Heilbronner, M Schrader, et al.Endokrinologie|October 1, 1982
Amniotic fluid levels of 17 alpha-hydroxyprogesterone during human pregnancy: pre-natal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiencyK G Wurster, M B Ranke, H Heilbronner, et al.Human Genetics|January 1, 1984
Satellited Y chromosomes: structure, origin, and clinical significanceM Schmid, T Haaf, E Solleder, et al.Biochemical and Biophysical Research Communications|November 14, 1984
Cell fusion responsible for horizontal oncogenesis by human tumors in nude miceJ Kömpf, H J Staab, H Heilbronner, et al.Human Genetics|February 1, 1991
Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenitaM Stuhrmann, H Heilbronner, A Reis, et al.Human Genetics|January 1, 1980
Data on linkage relations between GLO and 21-hydroxylaseJ Kömpf, G Siebert, H Ritter, et al.Pageof 2