Dr. Philip D. Cotter PHD, FACMG
Geneticist | Clinical Molecular Genetics
5810 Nancy Ridge Dr San Diego CA, 92121About
Dr. Philip Cotter practices Genetic Medicine in San Diego, CA. As a geneticist, Dr. Cotter 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. Cotter 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- Identification and disruption of lisRK, a genetic locus encoding a two-component signal transduction system involved in stress tolerance and virulence in Listeria monocytogenes.
- Monosomy 16 as the sole abnormality in myeloid malignancies.
- Mild phenotype in two siblings with distal monosomy 12p13.31-->pter.
- Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: identification of a candidate region for CFC syndrome.
- Candidate region for Coffin-Siris syndrome at 7q32-->34.
- Tetrasomy 15q25-->qter: cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome.
- Telomere-telomere (end to end) fusion of chromosomes 7 and 22 with an interstitial deletion of chromosome 7p11.2-->p15.1: phenotypic consequences and possible mechanisms.
- Analysis of the role of the Listeria monocytogenes F0F1 -AtPase operon in the acid tolerance response.
- Trisomy 4 and double minutes in acute myeloid leukemia: further evidence that double minutes can occur as the primary cytogenetic abnormality.
- Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier.
- Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
- A glutamate decarboxylase system protects Listeria monocytogenes in gastric fluid.
- Inherited duplication of Xq27.2-->qter: phenocopy of infantile Prader-Willi syndrome.
- Candidate region for cardio-facio-cutaneous syndrome.
- Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4.
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