Last Posted: Jul 31, 2019
- Re: An Analysis of the Frequency of Y-Chromosome Microdeletions and the Determination of a Threshold Sperm Concentration for Genetic Testing in Infertile Men.
Niederberger Craig et al. The Journal of urology 2019 202(2) 196-197 - Protocols for Genetic and Epigenetic Studies of Rare Diseases Affecting Dental Tissues.
Amorim Bruna Rabelo et al. Methods in molecular biology (Clifton, N.J.) 2019 1922453-492 - Study reveals elevated cancer risk in children with birth defects,
EurekAlert, June 25, 2019 - Zika Birth Defects Surveillance
CDC, 2019 - "Yeah that Made a Big Difference!": The Importance of the Relationship between Health Professionals and Fathers Who Have a Child with Down Syndrome.
Docherty Freyja et al. Journal of genetic counseling 2018 27(3) 665-674 - Pathogenic gene screening in 91 Chinese patients with short stature of unknown etiology with a targeted next-generation sequencing panel.
Yang Lulu et al. BMC medical genetics 2018 19(1) 212 - Non-invasive prenatal testing for detection of trisomy 13, 18, 21 and sex chromosome aneuploidies in 8594 cases.
Zheng Yunyun et al. Ginekologia polska 2019 90(5) 270-273 - Molecular Genetics of Noonan Syndrome and RASopathies.
Liao Jun et al. Pediatric endocrinology reviews : PER 2019 May 16(Suppl 2) 435-446 - Evaluation of machine learning algorithms for improved risk assessment for Down's syndrome.
Koivu Aki et al. Computers in biology and medicine 2018 981-7 - Noninvasive prenatal test for FGFR3-related skeletal dysplasia based on next-generation sequencing and plasma cell-free DNA: Test performance analysis and feasibility exploration.
Ren Yuan et al. Prenatal diagnosis 2018 38(11) 821-828
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