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Arthur R Brothman

Showing results (11-20 of 45) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2005
Section E6 of the ACMG technical standards and guidelines: chromosome studies for acquired abnormalitiesBetsy Hirsh, Arthur R Brothman, Peter B Jacky, et al.
Cancer Genetics and Cytogenetics|March 14, 2007
An inv(16) in Ph-negative cells of a chronic myelogenous leukemia patient after imatinib treatmentLeslie R Rowe, Arthur R Brothman, William E Nibley, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene clusterDavid A Stevenson, Steven B Bleyl, Teresa Maxwell, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|March 31, 2010
Evaluation of LOINC for representing constitutional cytogenetic test result reportsYan Z Heras, Joyce A Mitchell, Marc S Williams, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
A new genomic mechanism leading to cri-du-chat syndromeSarah T South, Jeffrey J Swensen, Teresa Maxwell, et al.
Obstetrics and Gynecology|February 20, 2010
Array comparative genomic hybridization for genetic evaluation of fetal loss between 10 and 20 weeks of gestationJennifer E Warren, David K Turok, Teresa M Maxwell, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotypeSarah T South, Heidi Whitby, Teresa Maxwell, et al.
Journal of Pediatric Hematology/Oncology|January 25, 2003
Her-2/neu expression in osteosarcoma increases risk of lung metastasis and can be associated with gene amplificationHolly Zhou, R Lor Randall, Arthur R Brothman, et al.
American Journal of Medical Genetics. Part A|January 27, 2005
Interstitial deletion 8q11.2-q13 with congenital anomalies of CHARGE associationCammon B Arrington, Brett C Cowley, Daniel R Nightingale, et al.
The Journal of Pediatrics|December 8, 2004
4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotypeDavid A Stevenson, John C Carey, Brett C Cowley, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2005
Section E6 of the ACMG technical standards and guidelines: chromosome studies for acquired abnormalitiesBetsy Hirsh, Arthur R Brothman, Peter B Jacky, et al.
Cancer Genetics and Cytogenetics|March 14, 2007
An inv(16) in Ph-negative cells of a chronic myelogenous leukemia patient after imatinib treatmentLeslie R Rowe, Arthur R Brothman, William E Nibley, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene clusterDavid A Stevenson, Steven B Bleyl, Teresa Maxwell, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|March 31, 2010
Evaluation of LOINC for representing constitutional cytogenetic test result reportsYan Z Heras, Joyce A Mitchell, Marc S Williams, et al.
American Journal of Medical Genetics. Part A|November 15, 2006
A new genomic mechanism leading to cri-du-chat syndromeSarah T South, Jeffrey J Swensen, Teresa Maxwell, et al.
Obstetrics and Gynecology|February 20, 2010
Array comparative genomic hybridization for genetic evaluation of fetal loss between 10 and 20 weeks of gestationJennifer E Warren, David K Turok, Teresa M Maxwell, et al.
American Journal of Medical Genetics. Part A|September 18, 2008
Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotypeSarah T South, Heidi Whitby, Teresa Maxwell, et al.
Journal of Pediatric Hematology/Oncology|January 25, 2003
Her-2/neu expression in osteosarcoma increases risk of lung metastasis and can be associated with gene amplificationHolly Zhou, R Lor Randall, Arthur R Brothman, et al.
American Journal of Medical Genetics. Part A|January 27, 2005
Interstitial deletion 8q11.2-q13 with congenital anomalies of CHARGE associationCammon B Arrington, Brett C Cowley, Daniel R Nightingale, et al.
The Journal of Pediatrics|December 8, 2004
4p terminal deletion and 11p subtelomeric duplication detected by genomic microarray in a patient with Wolf-Hirschhorn syndrome and an atypical phenotypeDavid A Stevenson, John C Carey, Brett C Cowley, et al.
Pageof 5