PubMed Clinical Queries for "Genetic counseling"

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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 1641

• Complete elimination of a pathogenic homoplasmic mtDNA mutation in one generation.
  Brady L, Sadikovic B, Rupar CA, Tarnopolsky MA.Mitochondrion. 2018 Feb 1; . Epub 2018 Feb 1.
• Hyperphosphatemic Familial Tumoral Calcinosis
  Ramnitz MS, Gafni RI, Collins MT.GeneReviews^®. 1993-2018.2018 Feb 1
• Reproductive Decision Support: Preferences and Needs of Couples at Risk for Hereditary Cancer and Clinical Geneticists.
  Reumkens K, van Oudheusden AJG, Gietel-Habets JJG, Tummers MHE, de Die-Smulders CEM, van Osch LADM.J Genet Couns. 2018 Jan 25; . Epub 2018 Jan 25.
• Clinical study of hereditary ovarian cancer syndrome in Shandong province, East China.
  Sheng X, Zhong Y, Lu C, Peng J, Yu H, Guo J.Int J Gynaecol Obstet. 2018 Jan 23; . Epub 2018 Jan 23.
• Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.
  Biesecker BB, Lewis KL, Umstead KL, Johnston JJ, Turbitt E, Fishler KP, Patton JH, Miller IM, Heidlebaugh AR, Biesecker LG.JAMA Intern Med. 2018 Jan 22; . Epub 2018 Jan 22.

See all (1641)

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 571

• Hereditary leiomyomatosis and renal cell carcinoma: Case report and review of the literature.
  Natália F, Tiago O, Pedro O, Sandro G.Urol Ann. 2018 Jan-Mar; 10(1):108-110.
• Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.
  Biesecker BB, Lewis KL, Umstead KL, Johnston JJ, Turbitt E, Fishler KP, Patton JH, Miller IM, Heidlebaugh AR, Biesecker LG.JAMA Intern Med. 2018 Jan 22; . Epub 2018 Jan 22.
• Genetic Tests for Breast and Ovarian Cancer
  Juvet LK, Natvig Norderhaug I.2008 Feb.
• The genetics of Parkinson disease.
  Deng H, Wang P, Jankovic J.Ageing Res Rev. 2017 Dec 26; 42:72-85. Epub 2017 Dec 26.
• ACOG Committee Opinion No. 727 Summary: Cascade Testing: Testing Women For Known Hereditary Genetic Mutations Associated With Cancer.
  [No authors listed]Obstet Gynecol. 2018 Jan; 131(1):194-195.

See all (571)

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 22506

• Self-perceptions from people with Down syndrome in Japan.
  Wakai M, Takahashi R, Higashigawa S, Ikeda M, Yotsumoto J, Numabe H.J Hum Genet. 2018 Feb 15; . Epub 2018 Feb 15.
• Sleep disorders and Parkinson disease; lessons from genetics.
  Gan-Or Z, Alcalay RN, Rouleau GA, Postuma RB.Sleep Med Rev. 2018 Jan 31; . Epub 2018 Jan 31.
• Cell-free DNA for the detection of fetal aneuploidy.
  Goldwaser T, Klugman S.Fertil Steril. 2018 Feb; 109(2):195-200.
• A novel tissue-based ß-catenin gene and immunohistochemical analysis to exclude familial adenomatous polyposis among children with hepatoblastoma tumors.
  Dubbink HJ, Hollink IHIM, Avenca Valente C, Wang W, Liu P, Doukas M, van Noesel MM, Dinjens WNM, Wagner A, Smits R.Pediatr Blood Cancer. 2018 Feb 15; . Epub 2018 Feb 15.
• Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations.
  Rebbeck TR, Friebel TM, Friedman E, Hamann U, Huo D, Kwong A, Olah E, Olopade OI, Solano AR, Teo SH, et al.Hum Mutat. 2018 Feb 15; . Epub 2018 Feb 15.

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