Physician
Medical Genetics
Dr. Peter Jacky, PHD
|
|
Give Review
Peter Jacky practices Medical Genetics. Peter Jacky is a published MD. He published 25 publications, including: 'Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2.'
Publications
- Section E6.5 of the ACMG technical standards and guidelines: chromosome studies for solid tumor abnormalities.
- Guidance for fluorescence in situ hybridization testing in hematologic disorders.
- Section E6 of the ACMG technical standards and guidelines: chromosome studies for acquired abnormalities.
- Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laborator...
- Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation.
- Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect.
- Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2.
- Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation.
- Chromosomal fragile site expression in dogs: II. Expression in boxer dogs with mast cell tumors.
- Chromosomal fragile site expression in dogs: I. Breed specific differences.
- A novel Robertsonian translocation in a family of Walker hounds.
- The giemsa banding pattern of canine chromosomes, using a cell synchronization technique.
- Cytogenetic evaluation of four canine mast cell tumors.
- Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytes.
- FMC-HU-1-B: a lymphoma B-cell line with unusual characteristics.
- Heritable fragile sites on human chromosomes. XI. Factors affecting expression of fragile sites at 10q25, 16q22, and 17p12.
- Thymidylate synthetase inhibitors and fragile site expression in lymphocytes.
- Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23.
- Fragile sites in chromosomes: possible model for the study of spontaneous chromosome breakage.
- Fragile X chromosome and chromosome condensation.
- The fragile X chromosome: current methods.
- Interferon-inducible fragile site on chromosome 16.
- Expression in fibroblast culture of the satellited-X chromosome associated with familial sex-linked mental retardation.
- CFU-S in individual erythroid colonies derived in vitro from adult mouse marrow.
Doctors Specialties
- Clinical Cytogenetics
- Medical Genetics
Accepted Insurances
Helpful Reviews
Similar Doctors
|
|
Dr. Susan Hayflick, MD
 This Doctor is OpenDoctor Recommended.
 This doctor has more publications
|
|
|
Dr. Darrell J. Salk, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Jacob A. Reiss, MD
This Doctor is OpenDoctor Recommended.
This doctor has more publications
|
|
|
Dr. Everett W. Lovrien, MD
This Doctor is OpenDoctor Recommended.
This doctor has more publications
|
|
|
Dr. David M. Koeller, MD
This Doctor is OpenDoctor Recommended.
This doctor has more publications
|
|
|
Dr. Jonathan Zonana, MD
This Doctor is OpenDoctor Recommended.
This doctor has more publications
|
|
|
Dr. Susan B. Olson, PHD |
|
|
Dr. Osvaldo A. Schirripa, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Jone E. Sampson, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Dana K. Simpson, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Caleb C. Rogers, MD |
|
|
Neil R. Buist, MB CHB
This Doctor is OpenDoctor Recommended.
This doctor has more publications
|
|
|
Jaellah Thalberg |
|
|
Debra A. King, PT |