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Translational Pediatrics
|
February 7, 2017
The dilemma of diagnostic testing for Prader-Willi syndrome
Arabella Smith, Dorothy Hung
Annales De Genetique
|
April 2, 2003
Use of two FISH probes provides a cost-effective, simple protocol to exclude an imprinting centre defect in routine laboratory testing for suspected Prader-Willi and Angelman syndrome
Arabella Smith, Lisa Robson, Luke St Heaps
American Journal of Medical Genetics
|
November 29, 2002
Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH
Arabella Smith, Luke St Heaps, Lisa Robson
Cancer Genetics and Cytogenetics
|
August 19, 2007
Heterogeneity of PLAG1 gene rearrangements in pleomorphic adenoma
Jothy Kandasamy, Arabella Smith, Sara Diaz, et al.
Cancer Genetics and Cytogenetics
|
April 18, 2006
Three adults with acute lymphoblastic leukemia and dic(7;9)(p11.2;p11)
Arabella Smith, Praboth Das, John O'Reilly, et al.
Medical and Pediatric Oncology
|
July 13, 2002
Mucoepidermoid carcinoma of the bronchus in a 15-year-old girl with complex cytogenetic rearrangement involving 11q and over-expression of cyclin D1
Wade Barrett, Luke St Heaps, Sara Diaz, et al.
Pediatric Hematology and Oncology
|
September 10, 2002
Intermittent 20q- and consistent i(7q) in a patient with Shwachman-Diamond syndrome
Arabella Smith, Peter J Shaw, Boyd Webster, et al.
Pathology
|
April 19, 2003
Use of FISH in an aggressive diffuse large B cell lymphoma
Arabella Smith, Philippa Kirkpatrick, Luke St Heaps, et al.
American Journal of Mental Retardation : AJMR
|
April 7, 2006
Mortality in Prader-Willi syndrome
Stewart L Einfeld, Sophie J Kavanagh, Arabella Smith, et al.
Obesity (Silver Spring, Md.)
|
May 12, 2015
Postprandial metabolism in adults with Prader-Willi syndrome
Louise Purtell, Alexander Viardot, Lisa Sze, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Translational Pediatrics
|
February 7, 2017
The dilemma of diagnostic testing for Prader-Willi syndrome
Arabella Smith, Dorothy Hung
Annales De Genetique
|
April 2, 2003
Use of two FISH probes provides a cost-effective, simple protocol to exclude an imprinting centre defect in routine laboratory testing for suspected Prader-Willi and Angelman syndrome
Arabella Smith, Lisa Robson, Luke St Heaps
American Journal of Medical Genetics
|
November 29, 2002
Apparently unrelated cytogenetic abnormalities among 462 probands referred for the detection of del(22q) by FISH
Arabella Smith, Luke St Heaps, Lisa Robson
Cancer Genetics and Cytogenetics
|
August 19, 2007
Heterogeneity of PLAG1 gene rearrangements in pleomorphic adenoma
Jothy Kandasamy, Arabella Smith, Sara Diaz, et al.
Cancer Genetics and Cytogenetics
|
April 18, 2006
Three adults with acute lymphoblastic leukemia and dic(7;9)(p11.2;p11)
Arabella Smith, Praboth Das, John O'Reilly, et al.
Medical and Pediatric Oncology
|
July 13, 2002
Mucoepidermoid carcinoma of the bronchus in a 15-year-old girl with complex cytogenetic rearrangement involving 11q and over-expression of cyclin D1
Wade Barrett, Luke St Heaps, Sara Diaz, et al.
Pediatric Hematology and Oncology
|
September 10, 2002
Intermittent 20q- and consistent i(7q) in a patient with Shwachman-Diamond syndrome
Arabella Smith, Peter J Shaw, Boyd Webster, et al.
Pathology
|
April 19, 2003
Use of FISH in an aggressive diffuse large B cell lymphoma
Arabella Smith, Philippa Kirkpatrick, Luke St Heaps, et al.
American Journal of Mental Retardation : AJMR
|
April 7, 2006
Mortality in Prader-Willi syndrome
Stewart L Einfeld, Sophie J Kavanagh, Arabella Smith, et al.
Obesity (Silver Spring, Md.)
|
May 12, 2015
Postprandial metabolism in adults with Prader-Willi syndrome
Louise Purtell, Alexander Viardot, Lisa Sze, et al.
Page
of 2