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
KMT2B -Related DystoniaAbela L, Kurian MA. GeneReviews<sup>®</sup>. 1993-2018. 2018 Apr 26
High-throughput non-invasive prenatal testing for fetal rhesus D status in RhD-negative women not known to be sensitised to the RhD antigen: a systematic review and economic evaluation. Saramago P, Yang H, Llewellyn A, Walker R, Harden M, Palmer S, Griffin S, Simmonds M. Health Technol Assess. 2018 Mar; 22(13):1-172.
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Kurahashi H, Hirose S. GeneReviews<sup>®</sup>. 1993-2018. 2002 May 16 [updated 2018 Mar 15]
Pulse oximetry screening for critical congenital heart defects. Plana MN, Zamora J, Suresh G, Fernandez-Pineda L, Thangaratinam S, Ewer AK. Cochrane Database Syst Rev. 2018 Mar 1; 3:CD011912. Epub 2018 Mar 1.
Loeys-Dietz Syndrome Loeys BL, Dietz HC. GeneReviews<sup>®</sup>. 1993-2018. 2008 Feb 28 [updated 2018 Mar 1]
See all (1488) 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 .
Ethics of routine: a critical analysis of the concept of 'routinisation' in prenatal screening. Kater-Kuipers A, de Beaufort ID, Galjaard RH, Bunnik EM. J Med Ethics. 2018 Apr 25; . Epub 2018 Apr 25.
High-throughput non-invasive prenatal testing for fetal rhesus D status in RhD-negative women not known to be sensitised to the RhD antigen: a systematic review and economic evaluation. Saramago P, Yang H, Llewellyn A, Walker R, Harden M, Palmer S, Griffin S, Simmonds M. Health Technol Assess. 2018 Mar; 22(13):1-172.
Non-Invasive Prenatal Test (NIPT) for Identification of Trisomy 21, 18 and 13 Juvet LK, Ormstad SS, Stoinska‐Schneider A, Solberg B, Arentz‐Hansen H, Kvamme MK, Fure B. 2016 Dec 16.
Non‐Invasive Prenatal Testing (NIPT) for Fetal Sex Determination. Health Technology Assessment Ormstad SS, Stoinska‐Schneider A, Solberg B, Fure B, Juvet LK. 2016 Dec 13.
Pulse oximetry screening for critical congenital heart defects. Plana MN, Zamora J, Suresh G, Fernandez-Pineda L, Thangaratinam S, Ewer AK. Cochrane Database Syst Rev. 2018 Mar 1; 3:CD011912. Epub 2018 Mar 1.
See all (383) 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: All Diagnosis Differential Diagnosis Clinical Description Management Genetic Counseling Molecular Genetics Genetic Testing
Ethics of routine: a critical analysis of the concept of 'routinisation' in prenatal screening. Kater-Kuipers A, de Beaufort ID, Galjaard RH, Bunnik EM. J Med Ethics. 2018 Apr 25; . Epub 2018 Apr 25.
A novel association of campomelic dysplasia with hydrocephalus due to an unbalanced chromosomal translocation upstream of SOX9. Antwi P, Hong CS, Duran D, Sheng Chih J, Dong W, DiLuna M, Kahle KT. Cold Spring Harb Mol Case Stud. 2018 Apr 25; . Epub 2018 Apr 25.
Is carriership of a balanced translocation or inversion an indication for non-invasive prenatal testing? Srebniak MI, Vogel I, Van Opstal D. Expert Rev Mol Diagn. 2018 Apr 26; :1-3. Epub 2018 Apr 26.
Baller-Gerold Syndrome Van Maldergem L, Piard J, Larizza L, Wang LL. GeneReviews<sup>®</sup>. 1993-2018. 2007 Aug 13 [updated 2018 Apr 19]
Prenatal screening for genetic disorders: Suggested guidelines for the Indian Scenario. Phadke SR, Puri RD, Ranganath P. Indian J Med Res. 2017 Dec; 146(6):689-699.
See all (5528) This column displays citations pertaining to topics in medical genetics. See more
filter information .
No hay comentarios:
Publicar un comentario