Dr. Mark H. Lipson MD
Geneticist | Clinical Genetics (M.D.)
2025 Morse Ave Sacramento CA, 95825About
Dr. Mark Lipson practices Genetic Medicine in Sacramento, CA. As a geneticist, Dr. Lipson 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. Lipson carries out studies, tests, and counsels patients with genetic diseases.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Common neonatal syndromes.
- Radiological findings in Hallermann-Streiff syndrome: report of five cases and a review of the literature.
- Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.
- Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis.
- Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screening.
- Ruvalcaba-Myhre-Smith syndrome.
- Trisomy 14 mosaicism syndrome.
- Epstein-Barr virus infections during pregnancy. A prospective study and review of the literature.
- Marshall-Smith syndrome: two case reports and a review of pulmonary manifestations.
- Normal initial blood galactose levels in a newborn with galactosemia.
- Ruptured hepatic artery aneurysm and coronary artery aneurysms with myocardial infarction in a 14-year-old boy: new manifestations of mucocutaneous lymph node syndrome.
- Ultrasonography and nephrotomography in the presymptomatic diagnosis of dominantly inherited (adult-onset) polycystic kidney disease.
- Affinity of cystathionine beta-synthase for pyridoxal 5'-phosphate in cultured cells. A mechanism for pyridoxine-responsive homocystinuria.
- Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen gene.
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