Dr. Andrew Robert Zinn MD
Endocrinology-Diabetes | Endocrinology, Diabetes & Metabolism
5323 Harry Hines Blvd Dallas TX, 75390About
Dr. Andrew Zinn practices Endocrinology in Dallas, TX. Dr. Zinn specializes in preventing, diagnosing, and treating diseases related to hormone imbalance, and the bodys glands in the endocrine system. Endocrinologists are trained and certified to treat a variety of conditions, including menopause, diabetes, infertility, and thyroid disorders, among many others. Dr. Zinn examines patients, determines means of testing, diagnoses, and decides the best treatment methods.
Education and Training
University of Texas Southwestern Medical Center Southwestern Medical School 1988
Provider Details
Expert Publications
Data provided by the National Library of Medicine- New gene family defined by MORC, a nuclear protein required for mouse spermatogenesis.
- Profound obesity associated with a balanced translocation that disrupts the SIM1 gene.
- Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene.
- The Turner syndrome-associated neurocognitive phenotype maps to distal Xp.
- Assignment of microrchidia (Morc) to mouse chromosome 16 by interspecific backcross linkage analysis and human chromosome 3q13 using somatic cell hybrids and in situ hybridization.
- A fork in the road to fertility.
- The X chromosome and the ovary.
- Molecular analysis of genes on Xp controlling Turner syndrome and premature ovarian failure (POF).
- A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from his mother and neurofibromatosis type 1 from his father.
- Phenotypes Associated with SHOX Deficiency.
- Most X;autosome translocations associated with premature ovarian failure do not interrupt X-linked genes.
- Mesomelic and rhizomelic short stature: The phenotype of combined Leri-Weill dyschondrosteosis and achondroplasia or hypochondroplasia.
- Sim1 gene dosage modulates the homeostatic feeding response to increased dietary fat in mice.
- Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.
- The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome.
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