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 1657

• Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms.
  Höben IM, Hjeij R, Olbrich H, Dougherty GW, Nöthe-Menchen T, Aprea I, Frank D, Pennekamp P, Dworniczak B, Wallmeier J, et al.Am J Hum Genet. 2018 May 3; 102(5):973-984.
• Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.
  Shickh S, Clausen M, Mighton C, Casalino S, Joshi E, Glogowski E, Schrader KA, Scheer A, Elser C, Panchal S, et al.BMJ Open. 2018 Apr 26; 8(4):e021876. Epub 2018 Apr 26.
• KMT2B-Related Dystonia
  Abela L, Kurian MA.GeneReviews^®. 1993-2018.2018 Apr 26
• Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers.
  Pritchard AL, Johansson PA, Nathan V, Howlie M, Symmons J, Palmer JM, Hayward NK.PLoS One. 2018; 13(4):e0194098. Epub 2018 Apr 11.
• Randomized trial of proactive rapid genetic counseling versus usual care for newly diagnosed breast cancer patients.
  Schwartz MD, Peshkin BN, Isaacs C, Willey S, Valdimarsdottir HB, Nusbaum R, Hooker G, O'Neill S, Jandorf L, Kelly SP, et al.Breast Cancer Res Treat. 2018 Apr 2; . Epub 2018 Apr 2.

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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 579

• The Challenge of Evaluating Adnexal Masses in Patients With Breast Cancer.
  Reinert T, Nogueira-Rodrigues A, Kestelman FP, Ashton-Prolla P, Graudenz MS, Bines J.Clin Breast Cancer. 2018 Mar 12; . Epub 2018 Mar 12.
• [Genetic diagnosis of Caroli syndrome with autosomal recessive polycystic kidney disease: a case report and literature review].
  Yang XY, Zhu LP, Liu XQ, Zhang CY, Yao Y, Wu Y.Beijing Da Xue Xue Bao Yi Xue Ban. 2018 Apr 18; 50(2):335-339.
• Children and young people's understanding of inherited conditions and their attitudes towards genetic testing: A systematic review.
  McGill BC, Wakefield CE, Vetsch J, Barlow-Stewart K, Kasparian NA, Patenaude AF, Young MA, Cohn RJ, Tucker KM.Clin Genet. 2018 Mar 25; . Epub 2018 Mar 25.
• Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.
  Hussein N, Weng SF, Kai J, Kleijnen J, Qureshi N.Cochrane Database Syst Rev. 2018 Mar 14; 3:CD010849. Epub 2018 Mar 14.
• Current practice for genetic counselling by nurses: An integrative review.
  Barr JA, Tsai LP, Welch A, Faradz SMH, Lane-Krebs K, Howie V, Hillman W.Int J Nurs Pract. 2018 Apr; 24(2):e12629. Epub 2018 Feb 20.

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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 22768

• Recurrent rhabdomyolysis caused by carnitine palmitoyltransferase II deficiency, common but under-recognised: Lessons to be learnt.
  Balasubramanian M, Jenkins TM, Kirk RJ, Nesbitt IM, Olpin SE, Hill M, Gillett GT.Mol Genet Metab Rep. 2018 Jun; 15:69-70. Epub 2018 Mar 6.
• Validation of Version 3.0 of the Breast Cancer Genetics Referral Screening Tool (B-RST™).
  Bellcross C, Hermstad A, Tallo C, Stanislaw C.Genet Med. 2018 May 8; . Epub 2018 May 8.
• Clinical providers' experiences with returning results from genomic sequencing: an interview study.
  Wynn J, Lewis K, Amendola LM, Bernhardt BA, Biswas S, Joshi M, McMullen C, Scollon S.BMC Med Genomics. 2018 May 8; 11(1):45. Epub 2018 May 8.
• Molecular Cytogenetic Diagnostics of Marker Chromosomes: Analysis in Four Prenatal Cases and Long-Term Clinical Evaluation of Carriers.
  Tesner P, Vlckova M, Drabova J, Vseticka J, Klimova A, Lastuvkova J, Zidovska J, Kremlikova Pourova R, Hancarova M, Sedlacek Z, et al.Cytogenet Genome Res. 2018 May 9; . Epub 2018 May 9.
• Novel PLS3 variants in X-linked osteoporosis: Exploring bone material properties.
  Balasubramanian M, Fratzl-Zelman N, O'Sullivan R, Bull M, Fa Peel N, Pollitt RC, Jones R, Milne E, Smith K, Roschger P, et al.Am J Med Genet A. 2018 May 7; . Epub 2018 May 7.

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