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Showing results (341-350 of 391) with videos related to

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Leukemia|September 1, 1996
Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemiaB A van der Reijden, D Martinet, J G Dauwerse, et al.
Hormone Research in Paediatrics|October 11, 2014
Copy number variants in short children born small for gestational ageJan M Wit, Hermine A van Duyvenvoorde, Jan B van Klinken, et al.
Human Molecular Genetics|August 21, 2018
Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneitiesMarian A J Weterman, Molly Kuo, Susan B Kenter, et al.
Human Mutation|July 31, 2010
Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2Emmelien Aten, Lisa C Brasz, Dorothea Bornholdt, et al.
Breast Cancer Research and Treatment|February 3, 2012
MUTYH gene variants and breast cancer in a Dutch case–control studyAstrid A Out, Marijke Wasielewski, Petra E A Huijts, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma familiesFemke A de Snoo, Jouke-Jan Hottenga, Elizabeth M Gillanders, et al.
American Journal of Human Genetics|October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acidKathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
Genomics|December 10, 1999
Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16O Le Saux, Z Urban, H H Göring, et al.
Familial Cancer|October 24, 2003
Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive casesY M C Hendriks, J T C M Verhallen, J J van der Smagt, et al.
Gastroenterology|February 14, 2006
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)Yvonne M C Hendriks, Shantie Jagmohan-Changur, Heleen M van der Klift, et al.
Pageof 40

Showing results (341-350 of 391) with videos related to

Sort By:
Pageof 40
Leukemia|September 1, 1996
Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemiaB A van der Reijden, D Martinet, J G Dauwerse, et al.
Hormone Research in Paediatrics|October 11, 2014
Copy number variants in short children born small for gestational ageJan M Wit, Hermine A van Duyvenvoorde, Jan B van Klinken, et al.
Human Molecular Genetics|August 21, 2018
Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneitiesMarian A J Weterman, Molly Kuo, Susan B Kenter, et al.
Human Mutation|July 31, 2010
Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2Emmelien Aten, Lisa C Brasz, Dorothea Bornholdt, et al.
Breast Cancer Research and Treatment|February 3, 2012
MUTYH gene variants and breast cancer in a Dutch case–control studyAstrid A Out, Marijke Wasielewski, Petra E A Huijts, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma familiesFemke A de Snoo, Jouke-Jan Hottenga, Elizabeth M Gillanders, et al.
American Journal of Human Genetics|October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acidKathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
Genomics|December 10, 1999
Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16O Le Saux, Z Urban, H H Göring, et al.
Familial Cancer|October 24, 2003
Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive casesY M C Hendriks, J T C M Verhallen, J J van der Smagt, et al.
Gastroenterology|February 14, 2006
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)Yvonne M C Hendriks, Shantie Jagmohan-Changur, Heleen M van der Klift, et al.
Pageof 40