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O Bartsch

Showing results (31-40 of 65) with videos related to

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Cancer Genetics and Cytogenetics|November 1, 1993
Partial trisomy of 3q detected by chromosome painting in a case of juvenile chronic myelomonocytic leukemiaK Michalová, O Bartsch, J Starý, et al.
American Journal of Medical Genetics|August 22, 2000
Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32-->qterI Talvik, K Ounap, O Bartsch, et al.
Genetic Counseling (Geneva, Switzerland)|February 7, 2012
A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 genesA O Caglayan, S Lechno, H Gumus, et al.
Regulatory Peptides|February 13, 2001
Bioactivity of recombinant prorelaxin from the marmoset monkeyR Zarreh-Hoshyari-Khah, O Bartsch, A Einspanier, et al.
American Journal of Medical Genetics|October 28, 1996
Evidence for a critical region for penoscrotal inversion, hypospadias, and imperforate anus within chromosomal region 13q32.2q34O Bartsch, U Kuhnle, L L Wu, et al.
Genetic Counseling (Geneva, Switzerland)|October 27, 2009
Rubinstein-Taybi syndrome and CREBBP c.201 202delTA mutation: a case presenting with varicella meningoencephalitisH Çaksen, O Bartsch, M Okur, et al.
American Journal of Medical Genetics|May 9, 2001
Burning down DEFECT11W Wuyts, W Van Hul, O Bartsch, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2003
A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletionE Morava, O Bartsch, M Czako, et al.
Cytogenetic and Genome Research|July 11, 2006
Two complementary recombinant chromosomes 5 in a healthy womanO Bartsch, M A Ergun, S Balci, et al.
American Journal of Medical Genetics|May 8, 1999
No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585O Bartsch, A Wagner, G K Hinkel, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Cancer Genetics and Cytogenetics|November 1, 1993
Partial trisomy of 3q detected by chromosome painting in a case of juvenile chronic myelomonocytic leukemiaK Michalová, O Bartsch, J Starý, et al.
American Journal of Medical Genetics|August 22, 2000
Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32-->qterI Talvik, K Ounap, O Bartsch, et al.
Genetic Counseling (Geneva, Switzerland)|February 7, 2012
A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 genesA O Caglayan, S Lechno, H Gumus, et al.
Regulatory Peptides|February 13, 2001
Bioactivity of recombinant prorelaxin from the marmoset monkeyR Zarreh-Hoshyari-Khah, O Bartsch, A Einspanier, et al.
American Journal of Medical Genetics|October 28, 1996
Evidence for a critical region for penoscrotal inversion, hypospadias, and imperforate anus within chromosomal region 13q32.2q34O Bartsch, U Kuhnle, L L Wu, et al.
Genetic Counseling (Geneva, Switzerland)|October 27, 2009
Rubinstein-Taybi syndrome and CREBBP c.201 202delTA mutation: a case presenting with varicella meningoencephalitisH Çaksen, O Bartsch, M Okur, et al.
American Journal of Medical Genetics|May 9, 2001
Burning down DEFECT11W Wuyts, W Van Hul, O Bartsch, et al.
Genetic Counseling (Geneva, Switzerland)|October 28, 2003
A girl with cutaneous hyperpigmentation, café au lait spots and ring chromosome 15 without significant deletionE Morava, O Bartsch, M Czako, et al.
Cytogenetic and Genome Research|July 11, 2006
Two complementary recombinant chromosomes 5 in a healthy womanO Bartsch, M A Ergun, S Balci, et al.
American Journal of Medical Genetics|May 8, 1999
No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585O Bartsch, A Wagner, G K Hinkel, et al.
Pageof 7