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G Schwanitz

Showing results (81-90 of 123) with videos related to

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Human Genetics|May 1, 1992
Chromosomal findings in fetuses with prenatally diagnosed cysts of the choroid plexusK Zerres, H Schüler, U Gembruch, et al.
Advances in Medical Sciences|March 16, 2007
Sperm analyses, genetic counselling and therapy in an infertile carrier of a supernumerary marker chromosome 15U Paetzold, G Schwanitz, R Schubert, et al.
Annales De Genetique|January 1, 1990
Prenatal detection of heart defects as an indication for chromosome analysisG Schwanitz, K Zerres, U Gembruch, et al.
Journal of Medical Genetics|July 25, 1998
Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibsD Wieczorek, H Engels, R Viersbach, et al.
Annales De Genetique|January 1, 1996
Further arguments for non-fortuitous association of Potter sequence with XYY malesS Rudnik-Schöneborn, H M Schüler, G Schwanitz, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1977
Partial deletion of 1q, following a pericentric inversion, in a boy with multiple minor morphologic anomalies and mental retardationG Schwanitz, P Schmid, C Hägele, et al.
Lancet (London, England)|January 13, 1990
Prenatal diagnosis of acute non-lymphoblastic leukaemia in Down syndromeK Zerres, G Schwanitz, M Niesen, et al.
Orvosi Hetilap|August 10, 2001
[Uniparental disomy 7 in the pathogenesis of Silver-Russell syndrome]S Mergenthaler, M Dobos, H Wollmann, et al.
Human Genetics|January 1, 1985
On the significance of true trisomy 20 mosaicism in amniotic fluid cultureM Djalali, P Steinbach, E Schwinger, et al.
Humangenetik|June 19, 1975
Partial monosomy 13 as the result of a balanced translocation 3/13 patG Schwanitz, M Reither, G Grosse, et al.
Pageof 13

Showing results (81-90 of 123) with videos related to

Sort By:
Pageof 13
Human Genetics|May 1, 1992
Chromosomal findings in fetuses with prenatally diagnosed cysts of the choroid plexusK Zerres, H Schüler, U Gembruch, et al.
Advances in Medical Sciences|March 16, 2007
Sperm analyses, genetic counselling and therapy in an infertile carrier of a supernumerary marker chromosome 15U Paetzold, G Schwanitz, R Schubert, et al.
Annales De Genetique|January 1, 1990
Prenatal detection of heart defects as an indication for chromosome analysisG Schwanitz, K Zerres, U Gembruch, et al.
Journal of Medical Genetics|July 25, 1998
Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibsD Wieczorek, H Engels, R Viersbach, et al.
Annales De Genetique|January 1, 1996
Further arguments for non-fortuitous association of Potter sequence with XYY malesS Rudnik-Schöneborn, H M Schüler, G Schwanitz, et al.
Acta Geneticae Medicae Et Gemellologiae|January 1, 1977
Partial deletion of 1q, following a pericentric inversion, in a boy with multiple minor morphologic anomalies and mental retardationG Schwanitz, P Schmid, C Hägele, et al.
Lancet (London, England)|January 13, 1990
Prenatal diagnosis of acute non-lymphoblastic leukaemia in Down syndromeK Zerres, G Schwanitz, M Niesen, et al.
Orvosi Hetilap|August 10, 2001
[Uniparental disomy 7 in the pathogenesis of Silver-Russell syndrome]S Mergenthaler, M Dobos, H Wollmann, et al.
Human Genetics|January 1, 1985
On the significance of true trisomy 20 mosaicism in amniotic fluid cultureM Djalali, P Steinbach, E Schwinger, et al.
Humangenetik|June 19, 1975
Partial monosomy 13 as the result of a balanced translocation 3/13 patG Schwanitz, M Reither, G Grosse, et al.
Pageof 13