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R D Wegner

Showing results (21-30 of 67) with videos related to

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Prenatal Diagnosis|March 1, 1988
Trisomy 14 mosaicism leading to cytogenetic discrepancies in chorionic villi sampled at different timesR D Wegner, R Hohle, G Karkut, et al.
Cytogenetic and Genome Research|September 7, 2006
Interphase M-FISH applications using commercial probes in prenatal and PGD diagnosticsM Stumm, R-D Wegner, M Bloechle, et al.
Experimental Cell Research|June 1, 1987
Monoclonal antibody with specificity to mitotic chromosomes of primatesF M Davis, R D Wegner, P N Rao
Humangenetik|January 1, 1975
Frequency and distribution of sister-chromatid exchanges in a case of Fanconi's anemiaK Sperling, R D Wegner, H Riehm, et al.
Clinical Genetics|December 1, 1996
Fanconi anemia complementation group E: clinical and cytogenetic data of the first patientR D Wegner, I Henrichs, H Joenje, et al.
Leukemia & Lymphoma|June 1, 1993
Partial trisomy 1q, an uncommon chromosomal aberration in erythroleukemiaE Baumgarten, R D Wegner, R Fengler, et al.
Clinical Genetics|August 1, 1992
Ring Y chromosome: cytogenetic and molecular characterizationR D Wegner, G Scherer, M Pohlschmidt, et al.
Der Urologe. Ausg. A|July 1, 1994
[Mixed gonadal dysgenesis--a rare cause of primary infertility. Report of 2 cases and review of the literature]H E Wegner, A Ferszt, R D Wegner, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1991
Frequency of trisomy 21 in Germany before and after the Chernobyl accidentK Sperling, J Pelz, R D Wegner, et al.
Padiatrie Und Padologie|January 1, 1986
Cri du chat-syndrome in combination with partial trisomy 9 pJ Sigmund, H Frisch, P Heinz-Erian, et al.
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|March 1, 1988
Trisomy 14 mosaicism leading to cytogenetic discrepancies in chorionic villi sampled at different timesR D Wegner, R Hohle, G Karkut, et al.
Cytogenetic and Genome Research|September 7, 2006
Interphase M-FISH applications using commercial probes in prenatal and PGD diagnosticsM Stumm, R-D Wegner, M Bloechle, et al.
Experimental Cell Research|June 1, 1987
Monoclonal antibody with specificity to mitotic chromosomes of primatesF M Davis, R D Wegner, P N Rao
Humangenetik|January 1, 1975
Frequency and distribution of sister-chromatid exchanges in a case of Fanconi's anemiaK Sperling, R D Wegner, H Riehm, et al.
Clinical Genetics|December 1, 1996
Fanconi anemia complementation group E: clinical and cytogenetic data of the first patientR D Wegner, I Henrichs, H Joenje, et al.
Leukemia & Lymphoma|June 1, 1993
Partial trisomy 1q, an uncommon chromosomal aberration in erythroleukemiaE Baumgarten, R D Wegner, R Fengler, et al.
Clinical Genetics|August 1, 1992
Ring Y chromosome: cytogenetic and molecular characterizationR D Wegner, G Scherer, M Pohlschmidt, et al.
Der Urologe. Ausg. A|July 1, 1994
[Mixed gonadal dysgenesis--a rare cause of primary infertility. Report of 2 cases and review of the literature]H E Wegner, A Ferszt, R D Wegner, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1991
Frequency of trisomy 21 in Germany before and after the Chernobyl accidentK Sperling, J Pelz, R D Wegner, et al.
Padiatrie Und Padologie|January 1, 1986
Cri du chat-syndrome in combination with partial trisomy 9 pJ Sigmund, H Frisch, P Heinz-Erian, et al.
Pageof 7