Last Posted: Mar 11, 2020
- [Clinical practice guidelines for hereditary non-syndromic deafness].
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Li Shanglin et al. Frontiers in neurology 2019 101351 - Clinical features of genetically confirmed patients with primary hyperoxaluria identified by clinical indication versus familial screening.
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Andersson Nadine G et al. Haemophilia : the official journal of the World Federation of Hemophilia 2020 Feb - Social and cultural influences on genetic screening programme acceptability: A mixed-methods study of the views of adults, carriers, and family members living with thalassemia in the UK.
Boardman Felicity K et al. Journal of genetic counseling 2020 Mar - Genetic Screening of the Patients with Primary Immunodeficiency by Whole-
B Erman et al, Ped Allergy Immunol Pulm,February 2020 - Clinical implications of mismatch repair deficiency in prostate cancer.
Sedhom Ramy et al. Future oncology (London, England) 2019 Jul 15(20) 2395-2411 - Fragile X-associated conditions: implications for the whole family.
McKechanie Andrew G et al. The British journal of general practice : the journal of the Royal College of General Practitioners 2019 Sep 69(686) 460-461 - Molecular and Histopathological Characterization of Patients Presenting with the Duchenne Muscular Dystrophy Phenotype in a Tertiary Care Center in Southern India.
Tallapaka Karthik et al. Indian pediatrics 2019 56(7) 556-559 - Relationship between phenotype and genotype of 102 Chinese newborns with Prader-Willi syndrome.
Ge Meng-Meng et al. Molecular biology reports 2019 Oct 46(5) 4717-4724
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