PubMed Clinical Queries for "Genetic counseling"

PubMed Clinical Queries



From PubMed Clinical Queries

PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas

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• Search PubMed Clinical Queries for "Genetic counseling" 

Results: 5 of 1708

• [Diagnosis and Treatment of MSI-H Cancer in Gynecological Cancer].
  Yamamoto N, Tashiro H, Katabuchi H.Gan To Kagaku Ryoho. 2018 Nov; 45(11):1577-1581.
• Preferences for in-person disclosure: Patients declining telephone disclosure characteristics and outcomes in the multi-center COGENT Study.
  Beri N, Patrick-Miller LJ, Egleston BL, Hall MJ, Domchek SM, Daly MB, Ganschow P, Grana G, Olopade OI, Fetzer D, et al.Clin Genet. 2018 Nov 12; . Epub 2018 Nov 12.
• Disparities in genetic services utilization in a random sample of young breast cancer survivors.
  Nikolaidis C, Duquette D, Mendelsohn-Victor KE, Anderson B, Copeland G, Milliron KJ, Merajver SD, Janz NK, Northouse LL, Duffy SA, et al.Genet Med. 2018 Nov 2; . Epub 2018 Nov 2.
• Identifying patients with a history of ovarian cancer for referral for genetic counselling: non-randomised comparison of two case-finding strategies in primary care.
  Helsper CW, Van Vliet LM, Velthuizen ME, de Wit NJ, Beijaert RP, Butter E, van Gent-Wagemakers MP, Witteveen EO, Zweemer RP, van Dulmen SM, et al.Br J Gen Pract. 2018 Nov; 68(676):e750-e756.
• Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study.
  Qian F, Wang S, Mitchell J, McGuffog L, Barrowdale D, Leslie G, Oosterwijk JC, Chung WK, Evans DG, Engel C, et al.J Natl Cancer Inst. 2018 Oct 12; . Epub 2018 Oct 12.

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This column displays citations filtered to a specific clinical study category and scope. These search filters were developed by Haynes RB et al. See more filter information.

Systematic Reviews

Results: 5 of 612

• Molecular genetics of the POMT1-related muscular dystrophy-dystroglycanopathies.
  Hu P, Yuan L, Deng H.Mutat Res. 2018 Oct - Dec; 778:45-50. Epub 2018 Sep 12.
• Spectrum of mutations of cystic fibrosis in the 22 Arab countries: A systematic review.
  Al-Sadeq D, Abunada T, Dalloul R, Fahad S, Taleb S, Aljassim K, Al Hamed FA, Zayed H.Respirology. 2018 Nov 12; . Epub 2018 Nov 12.
• What do people think about genetics? A systematic review.
  LePoire E, Basu B, Walker L, Bowen DJ.J Community Genet. 2018 Nov 7; . Epub 2018 Nov 7.
• Clinical and Genetic Characteristics of BRCA1/2 Mutation in Korean Ovarian Cancer Patients: A Multicenter Study and Literature Review.
  Kwon BS, Byun JM, Lee HJ, Jeong DH, Lee TH, Shin KH, Suh DS, Kim KH.Cancer Res Treat. 2018 Oct 8; . Epub 2018 Oct 8.
• Dermatoglyphic Analysis in Parents with Cleft Children: A Comparative Study.
  Harika DJ, Sridevi E, Sai Sankar AJ, Pranitha K, Gosla SR, Kiran GB.Contemp Clin Dent. 2018 Sep; 9(Suppl 2):S291-S298.

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This column displays citations for systematic reviews, meta-analyses, reviews of clinical trials, evidence-based medicine, consensus development conferences, and guidelines. See filter information or additional related sources.

Medical Genetics

Topic:AllDiagnosisDifferential DiagnosisClinical DescriptionManagementGenetic CounselingMolecular GeneticsGenetic Testing

Results: 5 of 23408

• Perceptions of parents of children with hearing loss of genetic origin in South Africa.
  Gardiner SA, Laing N, Mall S, Wonkam A.J Community Genet. 2018 Nov 21; . Epub 2018 Nov 21.
• Clinical Genetics of Polydactyly: An Updated Review.
  Umair M, Ahmad F, Bilal M, Ahmad W, Alfadhel M.Front Genet. 2018; 9:447. Epub 2018 Nov 6.
• Mutational and phenotypic spectrum of phenylalanine hydroxylase deficiency in Zhejiang Province, China.
  Chen T, Xu W, Wu D, Han J, Zhu L, Tong F, Yang R, Zhao Z, Jiang P, Shu Q.Sci Rep. 2018 Nov 20; 8(1):17137. Epub 2018 Nov 20.
• Mutation analysis and pathogenicity identification of Mucopolysaccharidosis type IVA in 8 south China families.
  Xie J, Pan J, Guo D, Pan W, Li R, Guo C, Du M, Jiang W, Guo Y.Gene. 2018 Nov 17; . Epub 2018 Nov 17.
• Molecular genetics of the POMT1-related muscular dystrophy-dystroglycanopathies.
  Hu P, Yuan L, Deng H.Mutat Res. 2018 Oct - Dec; 778:45-50. Epub 2018 Sep 12.

See all (23408)

This column displays citations pertaining to topics in medical genetics. See more filter information.