Publications by authors named "Preetha Markose"

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16q24.3 Microdeletions Disrupting Upstream Non-Coding Region of Cause KBG Syndrome.
Aiko Iwata-Otsubo, Alyssa L Rippert, Jorune Balciuniene, Sarah K Fiordaliso, Robert Chen, Preetha Markose

Genes (Basel)· January 2025

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WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.
Cara M Skraban, Constance F Wells, Preetha Markose, Megan T Cho, Addie I Nesbitt

Am J Hum Genet· July 2017

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ABCB6 RNA expression in leukemias--expression is low in acute promyelocytic leukemia and FLT3-ITD-positive acute myeloid leukemia.
Ajay Abraham, Sreeja Karathedath, Savitha Varatharajan, Preetha Markose, Ezhilarasi Chendamarai

Ann Hematol· March 2014

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International reporting scale of BCR-ABL1 fusion transcript in chronic myeloid leukemia: first report from India.
Poonkuzhali Balasubramanian, Ezhilarasi Chendamarai, Preetha Markose, Linda Fletcher, Susan Branford

Acta Haematol· May 2012

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Spectrum of BCR-ABL kinase domain mutations in patients with chronic myeloid leukemia from India with suspected resistance to imatinib-mutations are rare and have different distributions.
Preetha Markose, Ezhilarasi Chendamarai, Poonkuzhali Balasubramanian, Shaji Ramachandran Velayudhan, Vivi M Srivastava

Leuk Lymphoma· December 2009

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