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H Wyandt

Showing results (1-10 of 18) with videos related to

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Cancer Genetics and Cytogenetics|December 1, 1991
Report of a variant t(1;15;17)(p36;q22;q21.1) in a patient with acute promyelocytic leukemiaP Osella, H Wyandt, E Vosburgh, et al.
Cancer Genetics and Cytogenetics|March 1, 1992
Cytogenetic studies of eight squamous cell carcinomas of the head and neck. Deletion of 7q, a possible primary chromosomal eventP Osella, A Carlson, H Wyandt, et al.
American Journal of Medical Genetics|August 1, 1990
Transmission of ring 14 chromosome from mother to two sonsR Matalon, P Supple, H Wyandt, et al.
Acta Obstetricia Et Gynecologica Scandinavica|March 1, 1997
Evaluation of satellited Y chromosome (Yqs) detected during prenatal diagnosisB R Haddad, Y Huang, H Wyandt, et al.
Journal of Medical Genetics|December 1, 1996
Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24)B R Haddad, A E Lin, H Wyandt, et al.
American Journal of Medical Genetics|March 10, 2001
Dr. Ram Verma, cytogeneticist 1946-2000A Babu, H A Lubs, M Macera, et al.
Clinical Genetics|July 6, 2005
Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridizationH F L Mark, H Wyandt, X L Huang, et al.
American Journal of Medical Genetics|August 1, 1990
Interstitial deletion involving most of YqJ Skare, H Drwinga, H Wyandt, et al.
Cytogenetics and Cell Genetics|January 1, 1993
In situ hybridization applied to Waardenburg syndromeB L Wu, A Milunsky, H Wyandt, et al.
Virginia Medical|April 1, 1983
Fragile X-linked mental retardation, a new entity: case reportsT E Kelly, M A Shires, L Harris, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Cancer Genetics and Cytogenetics|December 1, 1991
Report of a variant t(1;15;17)(p36;q22;q21.1) in a patient with acute promyelocytic leukemiaP Osella, H Wyandt, E Vosburgh, et al.
Cancer Genetics and Cytogenetics|March 1, 1992
Cytogenetic studies of eight squamous cell carcinomas of the head and neck. Deletion of 7q, a possible primary chromosomal eventP Osella, A Carlson, H Wyandt, et al.
American Journal of Medical Genetics|August 1, 1990
Transmission of ring 14 chromosome from mother to two sonsR Matalon, P Supple, H Wyandt, et al.
Acta Obstetricia Et Gynecologica Scandinavica|March 1, 1997
Evaluation of satellited Y chromosome (Yqs) detected during prenatal diagnosisB R Haddad, Y Huang, H Wyandt, et al.
Journal of Medical Genetics|December 1, 1996
Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24)B R Haddad, A E Lin, H Wyandt, et al.
American Journal of Medical Genetics|March 10, 2001
Dr. Ram Verma, cytogeneticist 1946-2000A Babu, H A Lubs, M Macera, et al.
Clinical Genetics|July 6, 2005
Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridizationH F L Mark, H Wyandt, X L Huang, et al.
American Journal of Medical Genetics|August 1, 1990
Interstitial deletion involving most of YqJ Skare, H Drwinga, H Wyandt, et al.
Cytogenetics and Cell Genetics|January 1, 1993
In situ hybridization applied to Waardenburg syndromeB L Wu, A Milunsky, H Wyandt, et al.
Virginia Medical|April 1, 1983
Fragile X-linked mental retardation, a new entity: case reportsT E Kelly, M A Shires, L Harris, et al.
Pageof 2