Literature DB >> 9369868

The impact of birth defects and genetic diseases.

J G Hall.   

Abstract

Entities:  

Mesh：

Year:  1997        PMID： 9369868     DOI： 10.1001/archpedi.1997.02170480012002

Source DB:  PubMed          Journal:  Arch Pediatr Adolesc Med        ISSN： 1072-4710


× No keyword cloud information.
  7 in total

Review 1.  Whole-Exome Sequencing and Whole-Genome Sequencing in Critically Ill Neonates Suspected to Have Single-Gene Disorders.

Authors:  Laurie D Smith; Laurel K Willig; Stephen F Kingsmore
Journal:  Cold Spring Harb Perspect Med       Date:  2015-12-18       Impact factor: 6.915

2.  Proportion of malformations and genetic disorders among cases encountered at a high-care unit in a children's hospital.

Authors:  Akiko Soneda; Hideki Teruya; Noritaka Furuya; Hiroshi Yoshihashi; Keisuke Enomoto; Aki Ishikawa; Kiyoshi Matsui; Kenji Kurosawa
Journal:  Eur J Pediatr       Date:  2011-07-16       Impact factor: 3.183

3.  The impact of single gene and chromosomal disorders on hospital admissions in an adult population.

Authors:  Danielle E Dye; Kate J Brameld; Susannah Maxwell; Jack Goldblatt; Peter O'Leary
Journal:  J Community Genet       Date:  2011-03-02

4.  The burden of genetic disease on inpatient care in a children's hospital.

Authors:  Shawn E McCandless; Jeanne W Brunger; Suzanne B Cassidy
Journal:  Am J Hum Genet       Date:  2003-12-12       Impact factor: 11.025

Review 5.  Rapid whole genome sequencing and precision neonatology.

Authors:  Joshua E Petrikin; Laurel K Willig; Laurie D Smith; Stephen F Kingsmore
Journal:  Semin Perinatol       Date:  2015-10-29       Impact factor: 3.300

Review 6.  Sequencing-based diagnostics for pediatric genetic diseases: progress and potential.

Authors:  Ahmad N Abou Tayoun; Bryan Krock; Nancy B Spinner
Journal:  Expert Rev Mol Diagn       Date:  2016-08-17       Impact factor: 5.225

7.  Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.

Authors:  Dimitri J Stavropoulos; Daniele Merico; Rebekah Jobling; Sarah Bowdin; Nasim Monfared; Bhooma Thiruvahindrapuram; Thomas Nalpathamkalam; Giovanna Pellecchia; Ryan K C Yuen; Michael J Szego; Robin Z Hayeems; Randi Zlotnik Shaul; Michael Brudno; Marta Girdea; Brendan Frey; Babak Alipanahi; Sohnee Ahmed; Riyana Babul-Hirji; Ramses Badilla Porras; Melissa T Carter; Lauren Chad; Ayeshah Chaudhry; David Chitayat; Soghra Jougheh Doust; Cheryl Cytrynbaum; Lucie Dupuis; Resham Ejaz; Leona Fishman; Andrea Guerin; Bita Hashemi; Mayada Helal; Stacy Hewson; Michal Inbar-Feigenberg; Peter Kannu; Natalya Karp; Raymond Kim; Jonathan Kronick; Eriskay Liston; Heather MacDonald; Saadet Mercimek-Mahmutoglu; Roberto Mendoza-Londono; Enas Nasr; Graeme Nimmo; Nicole Parkinson; Nada Quercia; Julian Raiman; Maian Roifman; Andreas Schulze; Andrea Shugar; Cheryl Shuman; Pierre Sinajon; Komudi Siriwardena; Rosanna Weksberg; Grace Yoon; Chris Carew; Raith Erickson; Richard A Leach; Robert Klein; Peter N Ray; M Stephen Meyn; Stephen W Scherer; Ronald D Cohn; Christian R Marshall
Journal:  NPJ Genom Med       Date:  2016-01-13       Impact factor: 8.617
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.