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S R Patil

Showing results (71-80 of 84) with videos related to

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Cancer Genetics and Cytogenetics|April 1, 1984
Evolution to eosinophilic leukemia with a t(5:11) translocation in a patient with idiopathic hypereosinophilic syndromeT J Yoo, S V Orman, S R Patil, et al.
Experimental Hematology|October 1, 1984
Marrow transplantation for stable-phase chronic granulocytic leukemiaJ O Armitage, L W Klassen, S R Patil, et al.
American Journal of Medical Genetics|January 1, 1981
Deletions of different segments of the long arm of chromosome 4J A Mitchell, S Packman, W D Loughman, et al.
Human Molecular Genetics|January 1, 1997
Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysisV C Sheffield, M E Pierpont, D Nishimura, et al.
Blood|October 15, 1990
Trisomy 13: a new recurring chromosome abnormality in acute leukemiaH Döhner, D C Arthur, E D Ball, et al.
Birth Defects Original Article Series|January 1, 1979
Chromosomal abnormalities ascertained in the collaborative perinatal survey of 7- and 8-year-old childrenH A Lubs, S R Patil, W J Kimberling, et al.
American Journal of Medical Genetics|July 9, 1999
Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal developmentD L Freedenberg, L W Gane, C S Richards, et al.
Nature Genetics|June 10, 1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25D Y Nishimura, R E Swiderski, W L Alward, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Cancer Research|September 29, 1998
Frequency of prolonged remission duration after high-dose cytarabine intensification in acute myeloid leukemia varies by cytogenetic subtypeC D Bloomfield, D Lawrence, J C Byrd, et al.
Pageof 9

Showing results (71-80 of 84) with videos related to

Sort By:
Pageof 9
Cancer Genetics and Cytogenetics|April 1, 1984
Evolution to eosinophilic leukemia with a t(5:11) translocation in a patient with idiopathic hypereosinophilic syndromeT J Yoo, S V Orman, S R Patil, et al.
Experimental Hematology|October 1, 1984
Marrow transplantation for stable-phase chronic granulocytic leukemiaJ O Armitage, L W Klassen, S R Patil, et al.
American Journal of Medical Genetics|January 1, 1981
Deletions of different segments of the long arm of chromosome 4J A Mitchell, S Packman, W D Loughman, et al.
Human Molecular Genetics|January 1, 1997
Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysisV C Sheffield, M E Pierpont, D Nishimura, et al.
Blood|October 15, 1990
Trisomy 13: a new recurring chromosome abnormality in acute leukemiaH Döhner, D C Arthur, E D Ball, et al.
Birth Defects Original Article Series|January 1, 1979
Chromosomal abnormalities ascertained in the collaborative perinatal survey of 7- and 8-year-old childrenH A Lubs, S R Patil, W J Kimberling, et al.
American Journal of Medical Genetics|July 9, 1999
Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal developmentD L Freedenberg, L W Gane, C S Richards, et al.
Nature Genetics|June 10, 1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25D Y Nishimura, R E Swiderski, W L Alward, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Cancer Research|September 29, 1998
Frequency of prolonged remission duration after high-dose cytarabine intensification in acute myeloid leukemia varies by cytogenetic subtypeC D Bloomfield, D Lawrence, J C Byrd, et al.
Pageof 9