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Syed M Jalal

Showing results (11-20 of 28) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 19, 2011
Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: a retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridizationBrandon M Shearer, Erik C Thorland, Austin W Carlson, et al.
American Journal of Medical Genetics. Part A|April 6, 2005
Subtelomere deletions and translocations are frequently familialAdewale Adeyinka, S Annie Adams, Cindy P Lorentz, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 17, 2005
Molecular diagnosis of Ewing's sarcoma/primitive neuroectodermal tumor in formalin-fixed paraffin-embedded tissues by RT-PCR and fluorescence in situ hybridizationXiang Qian, Long Jin, Brandon M Shearer, et al.
Journal of Cellular Biochemistry|September 5, 2002
Further characterization of human fetal osteoblastic hFOB 1.19 and hFOB/ER alpha cells: bone formation in vivo and karyotype analysis using multicolor fluorescent in situ hybridizationM Subramaniam, Syed M Jalal, David J Rickard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2004
Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3MbAdewale Adeyinka, Kimberly J Stockero, Heather C Flynn, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomaliesRegina E Ensenauer, William J Shaughnessy, Syed M Jalal, et al.
Diseases of the Colon and Rectum|October 18, 2005
Familial adenomatous polyposis and mental retardation caused by a de novo chromosomal deletion at 5q15-q22: report of a caseRobert Finch, Harvey G Moore, Noralane Lindor, et al.
Clinical Dysmorphology|January 7, 2003
Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25-->qter and monosomy 18p11.3-->pter in a girl with dysmorphic featuresGopalrao V N Velagaleti, Syed M Jalal, Ron C Michaelis, et al.
Journal of the American College of Cardiology|February 15, 2005
Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomaliesLuc M Beauchesne, Carole A Warnes, Heidi M Connolly, et al.
American Journal of Medical Genetics|March 14, 2002
Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delayBrynn Levy, Syed M Jalal, Teresa M Dunn, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 19, 2011
Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: a retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridizationBrandon M Shearer, Erik C Thorland, Austin W Carlson, et al.
American Journal of Medical Genetics. Part A|April 6, 2005
Subtelomere deletions and translocations are frequently familialAdewale Adeyinka, S Annie Adams, Cindy P Lorentz, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 17, 2005
Molecular diagnosis of Ewing's sarcoma/primitive neuroectodermal tumor in formalin-fixed paraffin-embedded tissues by RT-PCR and fluorescence in situ hybridizationXiang Qian, Long Jin, Brandon M Shearer, et al.
Journal of Cellular Biochemistry|September 5, 2002
Further characterization of human fetal osteoblastic hFOB 1.19 and hFOB/ER alpha cells: bone formation in vivo and karyotype analysis using multicolor fluorescent in situ hybridizationM Subramaniam, Syed M Jalal, David J Rickard, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2004
Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3MbAdewale Adeyinka, Kimberly J Stockero, Heather C Flynn, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomaliesRegina E Ensenauer, William J Shaughnessy, Syed M Jalal, et al.
Diseases of the Colon and Rectum|October 18, 2005
Familial adenomatous polyposis and mental retardation caused by a de novo chromosomal deletion at 5q15-q22: report of a caseRobert Finch, Harvey G Moore, Noralane Lindor, et al.
Clinical Dysmorphology|January 7, 2003
Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25-->qter and monosomy 18p11.3-->pter in a girl with dysmorphic featuresGopalrao V N Velagaleti, Syed M Jalal, Ron C Michaelis, et al.
Journal of the American College of Cardiology|February 15, 2005
Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomaliesLuc M Beauchesne, Carole A Warnes, Heidi M Connolly, et al.
American Journal of Medical Genetics|March 14, 2002
Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delayBrynn Levy, Syed M Jalal, Teresa M Dunn, et al.
Pageof 3