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W H Finley

Showing results (31-40 of 58) with videos related to

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Cancer Genetics and Cytogenetics|August 1, 1984
Translocation (9;11)(p21;q23) in a case of acute myeloblastic leukemia (AML-M2)A J Carroll, M C Poon, N C Robinson, et al.
The Journal of Pediatrics|October 1, 1972
Triploidy in a live-born male infantW H Finley, S C Finley, M B Green, et al.
Human Genetics|January 1, 1985
High resolution cytogenetic evaluation of couples with recurring fetal wastageT L Yang-Feng, S C Finley, W H Finley, et al.
Nucleic Acids Research|May 11, 1994
Over-representation of the disease associated (CAG) and (CGG) repeats in the human genomeJ Han, C Hsu, Z Zhu, et al.
Behavior Genetics|March 1, 1973
Prison survey for the XYY karyotype in tall inmatesW H Finley, C E McDanal, S C Finley, et al.
Journal of Medical Genetics|August 1, 1995
Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypesK M Keppler-Noreuil, A J Carroll, W H Finley, et al.
American Journal of Diseases of Children (1960)|August 1, 1981
Ring 4 chromosome with terminal p and q deletionsW H Finley, S C Finley, T Chonmaitree, et al.
American Journal of Medical Genetics|June 1, 1992
Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotypeN Krasikov, N Takaesu, T Hassold, et al.
American Journal of Medical Genetics|February 11, 1992
Autosomal dominant erythromelalgiaW H Finley, J R Lindsey, J D Fine, et al.
Journal of Medical Genetics|June 1, 1982
A complex chromosome rearrangement resulting in trisomy 15q22 to qterP N Howard-Peebles, P R Scarbrough, J Sharpe, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Cancer Genetics and Cytogenetics|August 1, 1984
Translocation (9;11)(p21;q23) in a case of acute myeloblastic leukemia (AML-M2)A J Carroll, M C Poon, N C Robinson, et al.
The Journal of Pediatrics|October 1, 1972
Triploidy in a live-born male infantW H Finley, S C Finley, M B Green, et al.
Human Genetics|January 1, 1985
High resolution cytogenetic evaluation of couples with recurring fetal wastageT L Yang-Feng, S C Finley, W H Finley, et al.
Nucleic Acids Research|May 11, 1994
Over-representation of the disease associated (CAG) and (CGG) repeats in the human genomeJ Han, C Hsu, Z Zhu, et al.
Behavior Genetics|March 1, 1973
Prison survey for the XYY karyotype in tall inmatesW H Finley, C E McDanal, S C Finley, et al.
Journal of Medical Genetics|August 1, 1995
Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypesK M Keppler-Noreuil, A J Carroll, W H Finley, et al.
American Journal of Diseases of Children (1960)|August 1, 1981
Ring 4 chromosome with terminal p and q deletionsW H Finley, S C Finley, T Chonmaitree, et al.
American Journal of Medical Genetics|June 1, 1992
Molecular and cytogenetic investigation of complex tissue-specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotypeN Krasikov, N Takaesu, T Hassold, et al.
American Journal of Medical Genetics|February 11, 1992
Autosomal dominant erythromelalgiaW H Finley, J R Lindsey, J D Fine, et al.
Journal of Medical Genetics|June 1, 1982
A complex chromosome rearrangement resulting in trisomy 15q22 to qterP N Howard-Peebles, P R Scarbrough, J Sharpe, et al.
Pageof 6