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Showing results (491-500 of 505) with videos related to

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BJOG : an International Journal of Obstetrics and Gynaecology|January 22, 2013
Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?D Ganesamoorthy, D L Bruno, G McGillivray, et al.
Prenatal Diagnosis|November 22, 2012
Application of a new molecular technique for the genetic evaluation of products of conceptionFrancesca R Grati, Denise Molina Gomes, Devika Ganesamoorthy, et al.
Leukemia|June 1, 2002
BFM-oriented treatment for children with acute lymphoblastic leukemia without cranial irradiation and treatment reduction for standard risk patients: results of DCLSG protocol ALL-8 (1991-1996)W A Kamps, J P M Bökkerink, F G A J Hakvoort-Cammel, et al.
Blood|August 10, 1999
Intensive treatment of children with acute lymphoblastic leukemia according to ALL-BFM-86 without cranial radiotherapy: results of Dutch Childhood Leukemia Study Group Protocol ALL-7 (1988-1991)W A Kamps, J P Bökkerink, K Hählen, et al.
Leukemia|March 23, 1999
Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7. European Working Group on MDS in Childhood (EWOG-MDS)H Hasle, M Aricò, G Basso, et al.
ACS Chemical Biology|August 17, 2012
Engineered luciferase reporter from a deep sea shrimp utilizing a novel imidazopyrazinone substrateMary P Hall, James Unch, Brock F Binkowski, et al.
Biomolecules|October 23, 2021
Confocal Endomicroscopy of Neuromuscular Junctions Stained with Physiologically Inert Protein Fragments of Tetanus ToxinCornelia Roesl, Elizabeth R Evans, Kosala N Dissanayake, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 13, 2012
Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation studyYoshimi Inaba, Amy S Herlihy, Charles E Schwartz, et al.
Molecular Autism|May 11, 2019
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresEmma K Baker, Marta Arpone, Solange M Aliaga, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
Pageof 51

Showing results (491-500 of 505) with videos related to

Sort By:
Pageof 51
BJOG : an International Journal of Obstetrics and Gynaecology|January 22, 2013
Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?D Ganesamoorthy, D L Bruno, G McGillivray, et al.
Prenatal Diagnosis|November 22, 2012
Application of a new molecular technique for the genetic evaluation of products of conceptionFrancesca R Grati, Denise Molina Gomes, Devika Ganesamoorthy, et al.
Leukemia|June 1, 2002
BFM-oriented treatment for children with acute lymphoblastic leukemia without cranial irradiation and treatment reduction for standard risk patients: results of DCLSG protocol ALL-8 (1991-1996)W A Kamps, J P M Bökkerink, F G A J Hakvoort-Cammel, et al.
Blood|August 10, 1999
Intensive treatment of children with acute lymphoblastic leukemia according to ALL-BFM-86 without cranial radiotherapy: results of Dutch Childhood Leukemia Study Group Protocol ALL-7 (1988-1991)W A Kamps, J P Bökkerink, K Hählen, et al.
Leukemia|March 23, 1999
Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7. European Working Group on MDS in Childhood (EWOG-MDS)H Hasle, M Aricò, G Basso, et al.
ACS Chemical Biology|August 17, 2012
Engineered luciferase reporter from a deep sea shrimp utilizing a novel imidazopyrazinone substrateMary P Hall, James Unch, Brock F Binkowski, et al.
Biomolecules|October 23, 2021
Confocal Endomicroscopy of Neuromuscular Junctions Stained with Physiologically Inert Protein Fragments of Tetanus ToxinCornelia Roesl, Elizabeth R Evans, Kosala N Dissanayake, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 13, 2012
Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation studyYoshimi Inaba, Amy S Herlihy, Charles E Schwartz, et al.
Molecular Autism|May 11, 2019
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresEmma K Baker, Marta Arpone, Solange M Aliaga, et al.
Journal of Medical Genetics|November 19, 2008
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practiceD L Bruno, D Ganesamoorthy, J Schoumans, et al.
Pageof 51