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P S Karnes

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Cancer Genetics and Cytogenetics|October 1, 1991
Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality, 46,XY,t(11;22)(p15.5;q11.23)P S Karnes, T N Tran, M Y Cui, et al.
Clinical Genetics|October 1, 1993
Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16N M Lindor, S M Jalal, S N Thibodeau, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 1, 2000
Familial occurrence of carcinoid tumors and association with other malignant neoplasmsD Babovic-Vuksanovic, C L Constantinou, J Rubin, et al.
Cancer Genetics and Cytogenetics|March 1, 1992
Cytogenetic analysis of 39 pediatric central nervous system tumorsP S Karnes, T N Tran, M Y Cui, et al.
Mayo Clinic Proceedings|July 1, 1992
Fluorescent in situ hybridization: use of whole chromosome paint probes to identify unbalanced chromosome translocationsW J Kraker, T J Borell, C R Schad, et al.
The Journal of Clinical Investigation|January 22, 2000
Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)S Kim, V Westphal, G Srikrishna, et al.
American Journal of Medical Genetics|August 28, 1995
Uniparental disomy in congenital disorders: a prospective studyN M Lindor, P S Karnes, V V Michels, et al.
The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Familial splenomegaly: macrophage hypercatabolism of lipoproteins associated with apolipoprotein E mutation [apolipoprotein E (delta149 Leu)]T T Nguyen, K E Kruckeberg, J F O'Brien, et al.
Genomics|October 14, 2000
Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genesF A Hol, M T Schepens, S E van Beersum, et al.
Journal of Medical Genetics|September 3, 2004
Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3N M Solomon, S A Ross, T Morgan, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Cancer Genetics and Cytogenetics|October 1, 1991
Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality, 46,XY,t(11;22)(p15.5;q11.23)P S Karnes, T N Tran, M Y Cui, et al.
Clinical Genetics|October 1, 1993
Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16N M Lindor, S M Jalal, S N Thibodeau, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 1, 2000
Familial occurrence of carcinoid tumors and association with other malignant neoplasmsD Babovic-Vuksanovic, C L Constantinou, J Rubin, et al.
Cancer Genetics and Cytogenetics|March 1, 1992
Cytogenetic analysis of 39 pediatric central nervous system tumorsP S Karnes, T N Tran, M Y Cui, et al.
Mayo Clinic Proceedings|July 1, 1992
Fluorescent in situ hybridization: use of whole chromosome paint probes to identify unbalanced chromosome translocationsW J Kraker, T J Borell, C R Schad, et al.
The Journal of Clinical Investigation|January 22, 2000
Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)S Kim, V Westphal, G Srikrishna, et al.
American Journal of Medical Genetics|August 28, 1995
Uniparental disomy in congenital disorders: a prospective studyN M Lindor, P S Karnes, V V Michels, et al.
The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Familial splenomegaly: macrophage hypercatabolism of lipoproteins associated with apolipoprotein E mutation [apolipoprotein E (delta149 Leu)]T T Nguyen, K E Kruckeberg, J F O'Brien, et al.
Genomics|October 14, 2000
Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genesF A Hol, M T Schepens, S E van Beersum, et al.
Journal of Medical Genetics|September 3, 2004
Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3N M Solomon, S A Ross, T Morgan, et al.
Pageof 2