Achandira M. Udayakumar

Muscat, MA, Oman

Last Updated: 09/26/2026

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Found 9 publications

First Cytogenetic Profile of Omani Patients with de novo Myelodysplastic Syndromes: Comparison with data from Asia, Africa, Europe and North and South America.

First Cytogenetic Profile of Omani Patients with de novo Myelodysplastic Syndromes: Comparison with data from Asia, Africa, Europe and North and South America.

Journal: Sultan Qaboos University medical journal

Published: February 25, 2016

Erratum to: Existing Challenges Associated with Offering Prenatal Genetic Diagnosis in an Arab Society in the Sultanate of Oman.

Erratum to: Existing Challenges Associated with Offering Prenatal Genetic Diagnosis in an Arab Society in the Sultanate of Oman.

Journal: Journal of genetic counseling

Published: January 06, 2015

Follicular Dendritic Cell Sarcoma: Cytogenetics and pathological findings.

Follicular Dendritic Cell Sarcoma: Cytogenetics and pathological findings.

Journal: Sultan Qaboos University medical journal

Published: December 23, 2014

De Novo Duplication of 7p21.1p22.2 in a Child with Autism Spectrum Disorder and Craniofacial Dysmorphism.

De Novo Duplication of 7p21.1p22.2 in a Child with Autism Spectrum Disorder and Craniofacial Dysmorphism.

Journal: Sultan Qaboos University medical journal

Published: December 14, 2014

Cri-du-chat syndrome.

Cri-du-chat syndrome.

Journal: The Indian journal of medical research

Published: December 10, 2014

Cytogenetic, clinical, and hematological features of pediatric myelodysplastic syndrome in Oman.

Cytogenetic, clinical, and hematological features of pediatric myelodysplastic syndrome in Oman.

Journal: Pediatric blood & cancer

Published: August 26, 2014

Myelodysplasia progressing to acute myeloid leukemia in monozygotic twins with monosomy 7 as sole abnormality.

Myelodysplasia progressing to acute myeloid leukemia in monozygotic twins with monosomy 7 as sole abnormality.

Journal: Leukemia & lymphoma

Published: March 07, 2014

Constitutional trisomy 8 mosaicism syndrome: case report and review.

Constitutional trisomy 8 mosaicism syndrome: case report and review.

Journal: Journal of pediatric genetics

Published: December 01, 2013

A rare case of de novo mosaicism: Deletion 18p and isochromosome 18q syndrome.

A rare case of de novo mosaicism: Deletion 18p and isochromosome 18q syndrome.

Journal: Journal of pediatric genetics

Published: September 01, 2013

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Last Updated: 09/26/2026