Dr. Bernice A Allitto PHD
Geneticist | Clinical Molecular Genetics
3400 Computer Dr Genzyme Genetics Mol Westborough MA, 01581About
Dr. Bernice Allitto practices Genetic Medicine in Westborough, MA. As a geneticist, Dr. Allitto performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients? with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Allitto carries out studies, tests, and counsels patients with genetic diseases.
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Cystic fibrosis and chromosome abnormalities associated with echogenic fetal bowel.
- Improved detection of cystic fibrosis mutations in the heterogeneous U.S. population using an expanded, pan-ethnic mutation panel.
- The I148T CFTR allele occurs on multiple haplotypes: a complex allele is associated with cystic fibrosis.
- Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4.
- CFTR mutation distribution among U.S. Hispanic and African American individuals: evaluation in cystic fibrosis patient and carrier screening populations.
- Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation.
- A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene.
- Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72,400 specimens.
- Recombination events suggest potential sites for the Huntington's disease gene.
- A family of DNA sequences is reproducibly rearranged in the somatic nucleus of Tetrahymena.
- A DNA segment encoding two genes very tightly linked to Huntington's disease.
- Micronucleus-specific DNA sequences in an amicronucleate mutant of Tetrahymena.
- Quantitation of immunoglobulins in the effusions of human ovarian epithelial neoplasms.
- Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.
- Clinical molecular genetic testing.
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