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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.
American Journal of Perinatology
|
February 2, 2006
Fetal pericardial teratoma: presentation of two cases and review of literature
Rima Bader, Lisa K Hornberger, Larry J Nijmeh, et al.
Clinical Dysmorphology
|
September 8, 2006
Duodenal and biliary atresia associated with facial, thyroid and auditory apparatus abnormalities: a new mandibulofacial dysostosis syndrome?
Gustavo H B Maegawa, David Chitayat, Susan Blaser, et al.
Pediatric Blood & Cancer
|
March 31, 2021
Tumor surveillance for children and adolescents with cancer predisposition syndromes: The psychosocial impact reported by adolescents and caregivers
Kalene van Engelen, Maru Barrera, Jonathan D Wasserman, et al.
Prenatal Diagnosis
|
January 27, 2024
Validation of low-pass genome sequencing for prenatal diagnosis
Chloe Mighton, Abdul Noor, Nicholas Watkins, et al.
Journal of the American Heart Association
|
June 4, 2013
Impact of prenatal risk factors on congenital heart disease in the current era
Alan Fung, Cedric Manlhiot, Sapna Naik, et al.
Journal of Medical Genetics
|
June 5, 2015
Prenatal genomic microarray and sequencing in Canadian medical practice: towards consensus
Janet A Buchanan, David Chitayat, Elena Kolomietz, et al.
Journal of Pediatric Genetics
|
August 15, 2018
Challenges in Diagnosing Rare Genetic Causes of Common In Utero Presentations: Report of Two Patients with Mucolipidosis Type II (I-Cell Disease)
Gregory Costain, Michal Inbar-Feigenberg, Maha Saleh, 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.
European Journal of Human Genetics : EJHG
|
March 4, 2011
TSEN54 mutations cause pontocerebellar hypoplasia type 5
Yasmin Namavar, David Chitayat, Peter G Barth, et al.
Page
of 36
Search research articles
Search
Showing results (181-190 of 353) with videos related to
Sort By:
Page
of 36
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.
American Journal of Perinatology
|
February 2, 2006
Fetal pericardial teratoma: presentation of two cases and review of literature
Rima Bader, Lisa K Hornberger, Larry J Nijmeh, et al.
Clinical Dysmorphology
|
September 8, 2006
Duodenal and biliary atresia associated with facial, thyroid and auditory apparatus abnormalities: a new mandibulofacial dysostosis syndrome?
Gustavo H B Maegawa, David Chitayat, Susan Blaser, et al.
Pediatric Blood & Cancer
|
March 31, 2021
Tumor surveillance for children and adolescents with cancer predisposition syndromes: The psychosocial impact reported by adolescents and caregivers
Kalene van Engelen, Maru Barrera, Jonathan D Wasserman, et al.
Prenatal Diagnosis
|
January 27, 2024
Validation of low-pass genome sequencing for prenatal diagnosis
Chloe Mighton, Abdul Noor, Nicholas Watkins, et al.
Journal of the American Heart Association
|
June 4, 2013
Impact of prenatal risk factors on congenital heart disease in the current era
Alan Fung, Cedric Manlhiot, Sapna Naik, et al.
Journal of Medical Genetics
|
June 5, 2015
Prenatal genomic microarray and sequencing in Canadian medical practice: towards consensus
Janet A Buchanan, David Chitayat, Elena Kolomietz, et al.
Journal of Pediatric Genetics
|
August 15, 2018
Challenges in Diagnosing Rare Genetic Causes of Common In Utero Presentations: Report of Two Patients with Mucolipidosis Type II (I-Cell Disease)
Gregory Costain, Michal Inbar-Feigenberg, Maha Saleh, 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.
European Journal of Human Genetics : EJHG
|
March 4, 2011
TSEN54 mutations cause pontocerebellar hypoplasia type 5
Yasmin Namavar, David Chitayat, Peter G Barth, et al.
Page
of 36