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Genome Research
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September 4, 2008
Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13)
Marzena Gajecka, Andrew J Gentles, Albert Tsai, et al.
Cancer Genetics and Cytogenetics
|
September 29, 2009
Deletions of chromosome arms 7p and 7q in adult acute myeloid leukemia: a marker chromosome confirmed by array comparative genomic hybridization
Kwang-Sook Woo, Kyung-Eun Kim, Kyeong-Hee Kim, et al.
Journal of Human Genetics
|
October 17, 2014
Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2)
Alina Teresa Midro, Barbara Panasiuk, Beata Stasiewicz-Jarocka, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2008
Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature
Philippe M Campeau, Nicholas Ah Mew, Lola Cartier, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Duplication of the STS region in males is a benign copy-number variant
Aubry Furrow, Aaron Theisen, Lea Velsher, et al.
Leukemia Research
|
March 20, 2010
Duplications of the long arm of both chromosome 1, dup(1)(q21q32), leading to tetrasomy 1q in myelodysplastic syndrome
Ji-Eun Kim, Kwang-Sook Woo, Kyung-Eun Kim, et al.
Hemoglobin
|
June 1, 2005
ATR-16 due to a de novo complex rearrangement of chromosome 16
Marta S Gallego, Gabriela Zelaya, Aurora S Feliu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 18, 2007
Microarray analysis for constitutional cytogenetic abnormalities
Lisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, et al.
Plos One
|
August 12, 2009
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome
Jill A Rosenfeld, Blake C Ballif, Ann Lucas, et al.
Human Genetics
|
November 15, 2018
Standards and guidelines for canine clinical genetic testing laboratories
Lisa G Shaffer, Kyle Sundin, Anja Geretschlaeger, et al.
Page
of 22
Search research articles
Search
Showing results (101-110 of 215) with videos related to
Sort By:
Page
of 22
Genome Research
|
September 4, 2008
Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13)
Marzena Gajecka, Andrew J Gentles, Albert Tsai, et al.
Cancer Genetics and Cytogenetics
|
September 29, 2009
Deletions of chromosome arms 7p and 7q in adult acute myeloid leukemia: a marker chromosome confirmed by array comparative genomic hybridization
Kwang-Sook Woo, Kyung-Eun Kim, Kyeong-Hee Kim, et al.
Journal of Human Genetics
|
October 17, 2014
Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2)
Alina Teresa Midro, Barbara Panasiuk, Beata Stasiewicz-Jarocka, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2008
Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature
Philippe M Campeau, Nicholas Ah Mew, Lola Cartier, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Duplication of the STS region in males is a benign copy-number variant
Aubry Furrow, Aaron Theisen, Lea Velsher, et al.
Leukemia Research
|
March 20, 2010
Duplications of the long arm of both chromosome 1, dup(1)(q21q32), leading to tetrasomy 1q in myelodysplastic syndrome
Ji-Eun Kim, Kwang-Sook Woo, Kyung-Eun Kim, et al.
Hemoglobin
|
June 1, 2005
ATR-16 due to a de novo complex rearrangement of chromosome 16
Marta S Gallego, Gabriela Zelaya, Aurora S Feliu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 18, 2007
Microarray analysis for constitutional cytogenetic abnormalities
Lisa G Shaffer, Arthur L Beaudet, Arthur R Brothman, et al.
Plos One
|
August 12, 2009
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome
Jill A Rosenfeld, Blake C Ballif, Ann Lucas, et al.
Human Genetics
|
November 15, 2018
Standards and guidelines for canine clinical genetic testing laboratories
Lisa G Shaffer, Kyle Sundin, Anja Geretschlaeger, et al.
Page
of 22