Endocrinology Medical News about RET genetic screening

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RET genetic screening in patients with medullary thyroid cancer: The Moroccan experience
Journal of Cancer Research and Therapeutics, 10/27/09

Abdelhakim A et al. – Germline RET gene mutations are well known to be the genetic causes of multiple endocrine neoplasia type 2 (MEN2) and may be identified by genetic screening. These preliminary data suggest that the RET mutation spectra observed in Moroccan patients with MEN2 are similar to those previously reported in other countries.

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Assessing the usefulness of a novel MRI-based breast density estimation algorithm in a cohort of women at high genetic risk of breast cancer: The UK MARIBS study
Breast Cancer Research, 11/17/09 Relevance Score: 67%

Utilization of Blood Spot Testing for Metabolic-Genetic Disorders in Honduras: Is it Time for Newborn Screening
Journal of Child Neurology, 10/28/09 Relevance Score: 66%

Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects
Cardiology in the Young, 10/22/09 Relevance Score: 66%

Genetics: Newborn screening for sickle cell anemia
Canadian Family Physician, 10/14/09 Relevance Score: 66%

Carrier screening and genetic counselling in beta-thalassemia
International Journal of Hematology, 10/12/09 Relevance Score: 66%