266 related articles for article (PubMed ID: 20494254)
1. Newborn screening for treatable genetic conditions: past, present and future.
Hiraki S; Green NS
Obstet Gynecol Clin North Am; 2010 Mar; 37(1):11-21. PubMed ID: 20494254
[TBL] [Abstract][Full Text] [Related]
2. Newborn screening: an overview.
Carreiro-Lewandowski E
Clin Lab Sci; 2002; 15(4):229-38. PubMed ID: 12776783
[TBL] [Abstract][Full Text] [Related]
3. A review of newborn screening in the era of tandem mass spectrometry: what's new for the pediatric neurologist?
Copeland S
Semin Pediatr Neurol; 2008 Sep; 15(3):110-6. PubMed ID: 18708000
[TBL] [Abstract][Full Text] [Related]
4. CDC Grand Rounds: Newborn screening and improved outcomes.
Centers for Disease Control and Prevention (CDC)
MMWR Morb Mortal Wkly Rep; 2012 Jun; 61(21):390-3. PubMed ID: 22647744
[TBL] [Abstract][Full Text] [Related]
5. Technological advances in genetic testing.
Mele C
J Pediatr Nurs; 2010 Oct; 25(5):444-7. PubMed ID: 20816569
[No Abstract] [Full Text] [Related]
6. Neonatal screening by DNA microarray: spots and chips.
Green NS; Pass KA
Nat Rev Genet; 2005 Feb; 6(2):147-51. PubMed ID: 15716909
[TBL] [Abstract][Full Text] [Related]
7. Fast genetic sequencing saves newborn lives.
Reardon S
Nature; 2014 Oct; 514(7520):13-4. PubMed ID: 25279893
[No Abstract] [Full Text] [Related]
8. Strategies and logistical requirements for efficient testing in genetic disease.
Jackson-Cook C; Pandya A
Clin Lab Med; 1995 Dec; 15(4):839-57. PubMed ID: 8838226
[TBL] [Abstract][Full Text] [Related]
9. The current revolution in newborn screening: new technology, old controversies.
Tarini BA
Arch Pediatr Adolesc Med; 2007 Aug; 161(8):767-72. PubMed ID: 17679658
[TBL] [Abstract][Full Text] [Related]
10. The child neurologist's role in newborn screening programs: a commentary.
Duffner PK
Semin Pediatr Neurol; 2008 Sep; 15(3):117-8. PubMed ID: 18708001
[No Abstract] [Full Text] [Related]
11. Application of medical genetics in Turkey.
Tunçbilek E; Ozgüç M
Turk J Pediatr; 2007; 49(4):353-9. PubMed ID: 18246734
[TBL] [Abstract][Full Text] [Related]
12. [More specific analyses in neonatal screening using DNA techniques].
Larsson A
Lakartidningen; 2002 Apr; 99(17):1927-8. PubMed ID: 12043414
[No Abstract] [Full Text] [Related]
13. Doctors explore research potential of blood samples from newborns.
Roehr B
BMJ; 2009 Sep; 339():b3984. PubMed ID: 19786491
[No Abstract] [Full Text] [Related]
14. Newborn health screenings.
Rueschhoff A
NCSL Legisbrief; 2012 Dec; 20(47):1-2. PubMed ID: 23460998
[No Abstract] [Full Text] [Related]
15. Expanded newborn screening for genetic and metabolic disorders: modeling costs and outcomes.
Hubbard HB
Nurs Econ; 2007; 25(6):345-52. PubMed ID: 18240836
[TBL] [Abstract][Full Text] [Related]
16. Parental Opinions about the Expansion of the Neonatal Screening Programme.
Detmar S; Dijkstra N; Nijsingh N; Rijnders M; Verweij M; Hosli E
Community Genet; 2008; 11(1):11-7. PubMed ID: 18196913
[TBL] [Abstract][Full Text] [Related]
17. The obstetrician's role in newborn metabolic screening: a physician survey.
Hasegawa LE; Au SM; Matsumoto CA
Hawaii Med J; 2005 Sep; 64(9):239-43, 253. PubMed ID: 16274162
[TBL] [Abstract][Full Text] [Related]
18. Newborn screening and genetic testing.
Lloyd-Puryear MA; Forsman I
J Obstet Gynecol Neonatal Nurs; 2002; 31(2):200-7. PubMed ID: 11926404
[TBL] [Abstract][Full Text] [Related]
19. Expanded newborn screening of inherited metabolic disorders by tandem mass spectrometry: clinical and laboratory aspects.
Garg U; Dasouki M
Clin Biochem; 2006 Apr; 39(4):315-32. PubMed ID: 16563365
[TBL] [Abstract][Full Text] [Related]
20. Newborn screening in Australia and New Zealand.
Webster D; ;
Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():69-70. PubMed ID: 15906698
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
