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K Sperling

Showing results (91-100 of 145) with videos related to

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Human Genetics|January 28, 1976
Cytogenetic investigations in a new case of Bloom's syndromeK Sperling, U Goll, J Kunze, et al.
Prenatal Diagnosis|August 1, 1996
Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term cultureR D Wegner, E Schröck, M Obladen, et al.
BMJ (Clinical Research Ed.)|July 16, 1994
Significant increase in trisomy 21 in Berlin nine months after the Chernobyl reactor accident: temporal correlation or causal relation?K Sperling, J Pelz, R D Wegner, et al.
Chromosoma|January 1, 1985
DNase I sensitivity in facultative and constitutive heterochromatinK Sperling, B S Kerem, R Goitein, et al.
BMJ (Clinical Research Ed.)|November 12, 1994
Fallout from Chernobyl. Authors stand by study that Chernobyl increased trisomy 21 in BerlinK Sperling, J Pelz, R D Wegner, et al.
Journal of Medical Genetics|December 24, 2005
Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17pS Türkmen, O Demirhan, K Hoffmann, et al.
Chromosoma|January 1, 1988
DNase I sensitivity of Microtus agrestis active, inactive and reactivated X chromosomes in mouse-Microtus cell hybridsB S Kerem, V Kottusch-Geiseler, V Kalscheuer, et al.
Ceskoslovenska Pediatrie|June 1, 1990
[Sex determination using the polymerase chain reaction method for amplification of DNA segments on the X and Y chromosomes]M Macek, I Böhm, L Arnold, et al.
Die Naturwissenschaften|October 29, 1999
Proving the authenticity of ancient DNA by comparative genomic hybridizationS Hummel, B Herrmann, J Rameckers, et al.
Cancer Research|April 28, 2001
Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL)R Varon, A Reis, G Henze, et al.
Pageof 15

Showing results (91-100 of 145) with videos related to

Sort By:
Pageof 15
Human Genetics|January 28, 1976
Cytogenetic investigations in a new case of Bloom's syndromeK Sperling, U Goll, J Kunze, et al.
Prenatal Diagnosis|August 1, 1996
Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term cultureR D Wegner, E Schröck, M Obladen, et al.
BMJ (Clinical Research Ed.)|July 16, 1994
Significant increase in trisomy 21 in Berlin nine months after the Chernobyl reactor accident: temporal correlation or causal relation?K Sperling, J Pelz, R D Wegner, et al.
Chromosoma|January 1, 1985
DNase I sensitivity in facultative and constitutive heterochromatinK Sperling, B S Kerem, R Goitein, et al.
BMJ (Clinical Research Ed.)|November 12, 1994
Fallout from Chernobyl. Authors stand by study that Chernobyl increased trisomy 21 in BerlinK Sperling, J Pelz, R D Wegner, et al.
Journal of Medical Genetics|December 24, 2005
Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17pS Türkmen, O Demirhan, K Hoffmann, et al.
Chromosoma|January 1, 1988
DNase I sensitivity of Microtus agrestis active, inactive and reactivated X chromosomes in mouse-Microtus cell hybridsB S Kerem, V Kottusch-Geiseler, V Kalscheuer, et al.
Ceskoslovenska Pediatrie|June 1, 1990
[Sex determination using the polymerase chain reaction method for amplification of DNA segments on the X and Y chromosomes]M Macek, I Böhm, L Arnold, et al.
Die Naturwissenschaften|October 29, 1999
Proving the authenticity of ancient DNA by comparative genomic hybridizationS Hummel, B Herrmann, J Rameckers, et al.
Cancer Research|April 28, 2001
Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL)R Varon, A Reis, G Henze, et al.
Pageof 15