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Publications by Venkata Padmalatha
Fetal Loss: A Genetic Insight of the De Novo Accessory Bi-Satellited Marker of Chromosome 22P
Journal of Genetic Syndromes & Gene Therapy
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Prenatal Diagnosis of a Satellited Chromosome 8p Results From a De Novo Cryptic Translocation Between Chromosomes 8 and 22
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A Masculinizing Syndrome Associated With a Doubly-Satellited Extra Chromosome.
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Satellited Chromosome 9 in a Boy With Multiple Anomalies
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Deleted Yq in the Sterile Son of a Man With a Satellited Y Chromosome (Yqs).
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Is Chromosome 9 Loss a Marker of Disease Recurrence in Transitional Cell Carcinoma of the Urinary Bladder?
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A De Novo Marker Chromosome Derived From 9p in a Patient With 9p Partial Duplication Syndrome and Autism Features: Genotype-Phenotype Correlation
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A Human De Novo Mutation inMYH10phenocopies the Loss of Function Mutation in Mice
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