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American Journal of Medical Genetics. Part A
|
February 25, 2015
Sex-discordant monochorionic twins with blood and tissue chimerism
David Rodriguez-Buritica, Kitiwan Rojnueangnit, Ludwine M Messiaen, et al.
Hematology/Oncology and Stem Cell Therapy
|
October 21, 2019
Outcomes of high-risk acute promyelocytic leukemia patients treated with arsenic trioxide (ATO)/all trans retinoic acid (ATRA) based induction and consolidation without maintenance phase: A case Series
Gaurav Shah, Fady M Mikhail, Kimo Bachiasvili, et al.
Molecular Genetics & Genomic Medicine
|
June 29, 2019
Menkes disease complicated by concurrent Koolen-de Vries syndrome (17q21.31 deletion)
Taylor Woodfin, Christine Stoops, Joseph B Philips, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 29, 2016
Section E6.5-6.8 of the ACMG technical standards and guidelines: chromosome studies of lymph node and solid tumor-acquired chromosomal abnormalities
Linda D Cooley, Cynthia C Morton, Warren G Sanger, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2015
Partial trisomy 21: a fifty-year follow-up visit
J Austin Hamm, Andrew J Carroll, Fady M Mikhail, et al.
Molecular and Clinical Oncology
|
February 14, 2018
Therapy-associated myelodysplastic syndrome with monosomy 7 arising in a Muir-Torre Syndrome patient carrying <i>SETBP1</i> mutation
David Ullman, Erin Baumgartner, Nicholas Wnukowski, et al.
American Journal of Medical Genetics. Part A
|
October 1, 2015
Cleft palate in a patient with the nested 22q11.2 LCR C to D deletion
Crescenda L Williams, Katherine R Nelson, John H Grant, et al.
American Journal of Medical Genetics. Part A
|
July 13, 2006
Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2)
Fady M Mikhail, Dawn McIlvried, R Lynn Holt, et al.
Clinical Dysmorphology
|
May 20, 2009
A new syndrome with Stargardt macular degeneration, abnormalities of the corpus callosum, mental retardation, and dysmorphic features: a case report of two siblings
Maria Descartes, Stuart A Royal, Judith Franklin, et al.
Clinical Lymphoma, Myeloma & Leukemia
|
July 7, 2011
A case of acute promyelocytic leukemia without RARα rearrangement and apparently normal cytogenetics
Christos Vaklavas, Mark R Steciuk, Yongsheng Ren, et al.
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Search research articles
Search
Showing results (21-30 of 74) with videos related to
Sort By:
Page
of 8
American Journal of Medical Genetics. Part A
|
February 25, 2015
Sex-discordant monochorionic twins with blood and tissue chimerism
David Rodriguez-Buritica, Kitiwan Rojnueangnit, Ludwine M Messiaen, et al.
Hematology/Oncology and Stem Cell Therapy
|
October 21, 2019
Outcomes of high-risk acute promyelocytic leukemia patients treated with arsenic trioxide (ATO)/all trans retinoic acid (ATRA) based induction and consolidation without maintenance phase: A case Series
Gaurav Shah, Fady M Mikhail, Kimo Bachiasvili, et al.
Molecular Genetics & Genomic Medicine
|
June 29, 2019
Menkes disease complicated by concurrent Koolen-de Vries syndrome (17q21.31 deletion)
Taylor Woodfin, Christine Stoops, Joseph B Philips, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 29, 2016
Section E6.5-6.8 of the ACMG technical standards and guidelines: chromosome studies of lymph node and solid tumor-acquired chromosomal abnormalities
Linda D Cooley, Cynthia C Morton, Warren G Sanger, et al.
American Journal of Medical Genetics. Part A
|
May 7, 2015
Partial trisomy 21: a fifty-year follow-up visit
J Austin Hamm, Andrew J Carroll, Fady M Mikhail, et al.
Molecular and Clinical Oncology
|
February 14, 2018
Therapy-associated myelodysplastic syndrome with monosomy 7 arising in a Muir-Torre Syndrome patient carrying <i>SETBP1</i> mutation
David Ullman, Erin Baumgartner, Nicholas Wnukowski, et al.
American Journal of Medical Genetics. Part A
|
October 1, 2015
Cleft palate in a patient with the nested 22q11.2 LCR C to D deletion
Crescenda L Williams, Katherine R Nelson, John H Grant, et al.
American Journal of Medical Genetics. Part A
|
July 13, 2006
Complete trisomy 17p syndrome in a girl with der(14)t(14;17)(p11.2;p11.2)
Fady M Mikhail, Dawn McIlvried, R Lynn Holt, et al.
Clinical Dysmorphology
|
May 20, 2009
A new syndrome with Stargardt macular degeneration, abnormalities of the corpus callosum, mental retardation, and dysmorphic features: a case report of two siblings
Maria Descartes, Stuart A Royal, Judith Franklin, et al.
Clinical Lymphoma, Myeloma & Leukemia
|
July 7, 2011
A case of acute promyelocytic leukemia without RARα rearrangement and apparently normal cytogenetics
Christos Vaklavas, Mark R Steciuk, Yongsheng Ren, et al.
Page
of 8