World Birth Defects Day | Features | CDC
Last Posted: Oct 18, 2018
- A comparison of family financial and employment impacts of fragile X syndrome, autism spectrum disorders, and intellectual disability.
Ouyang Lijing et al. Research in developmental disabilities 2014 Jul 35(7) 1518-27 - Clinical and genetic analysis of a rare syndrome associated with neoteny.
Walker Richard F et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 20(5) 495-502 - Potential role of "omics" technique in prenatal diagnosis of congenital heart defects.
Chen Lizhu et al. Clinica chimica acta; international journal of clinical chemistry 2018 Jul 482185-190 - [Screening for hotspot mutations associated with genetic hearing impairment in pregnant women and subsequent prenatal diagnosis in high risk pregnancies].
Yang K et al. Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2018 Sep 53(9) 645-649 - Duchenne Muscular Dystrophy Care Considerations
CDC, September 2018 - Cell-Free DNA Screening for Aneuploidy and Microdeletion Syndromes.
Shaffer Brian L et al. Obstetrics and gynecology clinics of North America 2018 Mar 45(1) 13-26 - Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry.
Utine Gülen Eda et al. European journal of obstetrics, gynecology, and reproductive biology 2018 Feb 22176-80 - Genetic diagnostics of inherited aortic diseases : Medical strategy analysis.
von Kodolitsch Y et al. Herz 2017 Aug 42(5) 459-467 - Massively parallel sequencing on human cleavage-stage embryos to detect chromosomal abnormality.
Zhou Zhi et al. European journal of medical genetics 2018 Jan 61(1) 34-42 - Screening for Aneuploidy in Multiple Gestations: The Challenges and Options.
Bender Whitney et al. Obstetrics and gynecology clinics of North America 2018 Mar 45(1) 41-53
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