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Stuart Schwartz

Showing results (31-40 of 73) with videos related to

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Prenatal Diagnosis|March 30, 2026
Cytogenetic and Microarray Analysis Follow-Up of PGT-A Mosaic and Sex Discrepant Embryos During Pregnancy: Absence of Confirmation and Follow-Up RecommendationsLaura A Kline, Vanessa A Nitibhon, Erica L Soster, et al.
American Journal of Medical Genetics. Part A|August 17, 2020
Deletion rescue resulting in segmental homozygosity: A mechanism underlying discordant NIPT resultsSamantha Caldwell, Katelynn Sagaser, Zoe Nelson, et al.
Nature Genetics|December 4, 2001
Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- miceClemencia Colmenares, Heidi A Heilstedt, Lisa G Shaffer, et al.
American Journal of Human Genetics|September 22, 2005
Meiotic synapsis proceeds from a limited number of subtelomeric sites in the human malePetrice W Brown, Luann Judis, E Ricky Chan, et al.
Annals of Human Genetics|July 1, 2004
Identification and molecular characterization of a de novo supernumerary ring chromosome 18 in a patient with Klippel-Trenaunay syndromeA Anil Timur, Azita Sadgephour, Michael Graf, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2004
Detection of deletions in de novo "balanced" chromosome rearrangements: further evidence for their role in phenotypic abnormalitiesCaroline Astbury, Laurie A Christ, David J Aughton, et al.
Human Molecular Genetics|April 2, 2009
Inverted duplications on acentric markers: mechanism of formationAndrea E Murmann, Donald F Conrad, Heather Mashek, et al.
American Journal of Medical Genetics. Part A|September 22, 2025
Detection of Isodisomy Utilizing SNP Microarray: Frequency, Ascertainment, and ImplicationsSharon Molinari, Niecy Williams, Gloria Haskell, et al.
Prenatal Diagnosis|April 1, 2024
Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomesMargriet Johansen, Gloria T Haskell, Alexandra Arreola, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCNRachel D Burnside, Sharon Molinari, Christina Botti, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
Prenatal Diagnosis|March 30, 2026
Cytogenetic and Microarray Analysis Follow-Up of PGT-A Mosaic and Sex Discrepant Embryos During Pregnancy: Absence of Confirmation and Follow-Up RecommendationsLaura A Kline, Vanessa A Nitibhon, Erica L Soster, et al.
American Journal of Medical Genetics. Part A|August 17, 2020
Deletion rescue resulting in segmental homozygosity: A mechanism underlying discordant NIPT resultsSamantha Caldwell, Katelynn Sagaser, Zoe Nelson, et al.
Nature Genetics|December 4, 2001
Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- miceClemencia Colmenares, Heidi A Heilstedt, Lisa G Shaffer, et al.
American Journal of Human Genetics|September 22, 2005
Meiotic synapsis proceeds from a limited number of subtelomeric sites in the human malePetrice W Brown, Luann Judis, E Ricky Chan, et al.
Annals of Human Genetics|July 1, 2004
Identification and molecular characterization of a de novo supernumerary ring chromosome 18 in a patient with Klippel-Trenaunay syndromeA Anil Timur, Azita Sadgephour, Michael Graf, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 17, 2004
Detection of deletions in de novo "balanced" chromosome rearrangements: further evidence for their role in phenotypic abnormalitiesCaroline Astbury, Laurie A Christ, David J Aughton, et al.
Human Molecular Genetics|April 2, 2009
Inverted duplications on acentric markers: mechanism of formationAndrea E Murmann, Donald F Conrad, Heather Mashek, et al.
American Journal of Medical Genetics. Part A|September 22, 2025
Detection of Isodisomy Utilizing SNP Microarray: Frequency, Ascertainment, and ImplicationsSharon Molinari, Niecy Williams, Gloria Haskell, et al.
Prenatal Diagnosis|April 1, 2024
Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomesMargriet Johansen, Gloria T Haskell, Alexandra Arreola, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCNRachel D Burnside, Sharon Molinari, Christina Botti, et al.
Pageof 8