Suzena A. Masih
UP 211007, India
Last Updated: 09/26/2026
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Found 10 publications
Advances in diagnostic approaches to Fasciola infection in animals and humans: An overviews.
Journal: Journal of helminthology
Published: January 25, 2024
Deciphering the molecular landscape of microcephaly in 87 Indian families by exome sequencing.
Journal: European journal of medical genetics
Published: January 05, 2022
Variable neurological phenotypes of homocystinuria caused by biallelic methylenetetrahydrofolate reductase variants.
Journal: Clinical dysmorphology
Published: November 30, 2021
COASY related pontocerebellar hypoplasia type 12: A common Indian mutation with expansion of the phenotypic spectrum.
Journal: American journal of medical genetics. Part A
Published: November 16, 2021
Genomic Variations in ATP7B Gene in Indian Patients with Wilson Disease.
Journal: Indian journal of pediatrics
Published: August 15, 2021
Molecular analysis of severe hemophilia B in Indian families: Identification of mutational hotspot and novel variants.
Journal: International journal of laboratory hematology
Published: May 29, 2021
Homozygosity stretches around homozygous mutations in autosomal recessive disorders: patients from nonconsanguineous Indian families.
Journal: Journal of genetics
Published: March 12, 2021
Twins with PEX7 related intellectual disability and cataract: Highlighting phenotypes of peroxisome biogenesis disorder 9B.
Journal: American journal of medical genetics. Part A
Published: August 28, 2020
Homozygous Missense Variation in PNPLA8 Causes Prenatal-Onset Severe Neurodegeneration.
Journal: Molecular syndromology
Published: August 14, 2020
Renpenning syndrome in an Indian patient.
Journal: American journal of medical genetics. Part A
Published: March 26, 2019
Showing 1-10 of 10
Last Updated: 09/26/2026