Last Posted: Nov 15, 2019
- Item of Interest: Now Available: NIH Research Plan on Fragile X and Associated Conditions
NIH, November 2019 - Fragile X syndrome carrier screening accompanied by genetic consultation has clinical utility in populations beyond those recommended by guidelines.
Johansen Taber Katherine et al. Molecular genetics & genomic medicine 2019 Nov e1024 - New genetic analysis improves diagnosis of intellectual disability
Karolinska Institute, November 11, 2019 - Fragile X syndrome carrier screening in pregnant women in Chinese Han population.
Hung Chia-Cheng et al. Scientific reports 2019 Oct 9(1) 15456 - Was the Human Genome Project a dud?
EF Torrey, Dallas Morning News, October 13, 2019 - [Prenatal diagnosis for 30 women carrying a FMR1 mutation].
Huang Wen et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 Sep 36(9) 866-869 - The wild west of prenatal genetic testing
A Ramchandani, Mashable, August 2019 - Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder.
Munnich Arnold et al. Molecular autism 2019 1033 - What to Tell a Parent Who Worries a Young Child Has Autism.
Estes Annette et al. JAMA psychiatry 2019 Aug - Preventive care services and health behaviors in children with fragile X syndrome.
Gilbertson Kendra E et al. Disability and health journal 2019 May
.png)
No hay comentarios:
Publicar un comentario