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Howard Martin

Showing results (31-40 of 39) with videos related to

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Ophthalmology. Retina|May 16, 2024
Peripapillary Hyperreflective Ovoid Mass-Like Structures in Stickler SyndromeTasneem Z Khatib, Antoine Safi, Thomas Ralph William Nixon, et al.
Cancer|November 15, 2007
Cancer in Appalachia, 2001-2003Phyllis A Wingo, Thomas C Tucker, Patricia M Jamison, et al.
European Journal of Immunology|October 1, 2015
Epigenetic analysis of regulatory T cells using multiplex bisulfite sequencingDaniel B Rainbow, Xin Yang, Oliver Burren, et al.
International Journal of Endocrinology|April 18, 2015
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysisAndrea Luchetti, Diana Walsh, Fay Rodger, et al.
The Journal of Molecular Diagnostics : JMD|July 14, 2015
Somatic Mutation Screening Using Archival Formalin-Fixed, Paraffin-Embedded Tissues by Fluidigm Multiplex PCR and Illumina SequencingMing Wang, Leire Escudero-Ibarz, Sarah Moody, et al.
American Journal of Human Genetics|May 27, 2005
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndromeLionel Willatt, James Cox, John Barber, et al.
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
The Journal of Clinical Endocrinology and Metabolism|August 16, 2016
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-SituAdeline K Nicholas, Eva G Serra, Hakan Cangul, et al.
Blood|May 9, 2019
Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disordersKate Downes, Karyn Megy, Daniel Duarte, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Ophthalmology. Retina|May 16, 2024
Peripapillary Hyperreflective Ovoid Mass-Like Structures in Stickler SyndromeTasneem Z Khatib, Antoine Safi, Thomas Ralph William Nixon, et al.
Cancer|November 15, 2007
Cancer in Appalachia, 2001-2003Phyllis A Wingo, Thomas C Tucker, Patricia M Jamison, et al.
European Journal of Immunology|October 1, 2015
Epigenetic analysis of regulatory T cells using multiplex bisulfite sequencingDaniel B Rainbow, Xin Yang, Oliver Burren, et al.
International Journal of Endocrinology|April 18, 2015
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysisAndrea Luchetti, Diana Walsh, Fay Rodger, et al.
The Journal of Molecular Diagnostics : JMD|July 14, 2015
Somatic Mutation Screening Using Archival Formalin-Fixed, Paraffin-Embedded Tissues by Fluidigm Multiplex PCR and Illumina SequencingMing Wang, Leire Escudero-Ibarz, Sarah Moody, et al.
American Journal of Human Genetics|May 27, 2005
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndromeLionel Willatt, James Cox, John Barber, et al.
Nature Genetics|August 15, 2006
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disabilityCharles Shaw-Smith, Alan M Pittman, Lionel Willatt, et al.
The Journal of Clinical Endocrinology and Metabolism|August 16, 2016
Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-SituAdeline K Nicholas, Eva G Serra, Hakan Cangul, et al.
Blood|May 9, 2019
Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disordersKate Downes, Karyn Megy, Daniel Duarte, et al.
Pageof 4