-
1
-
-
38049002155
-
Committee on Practice and Ambulatory Medicine and Bright Futures Steering Committee. Recommendations for preventive pediatric health care
-
Committee on Practice and Ambulatory Medicine and Bright Futures Steering Committee. Recommendations for preventive pediatric health care. Pediatrics 120 (2007) 1376
-
(2007)
Pediatrics
, vol.120
, pp. 1376
-
-
-
2
-
-
33846082765
-
Newborn screening: toward a uniform screening panel and system-executive summary
-
Watson M.S., Mann M.Y., Lloyd-Puryear M.A., et al. Newborn screening: toward a uniform screening panel and system-executive summary. Pediatrics 117 (2006) S296-S307
-
(2006)
Pediatrics
, vol.117
-
-
Watson, M.S.1
Mann, M.Y.2
Lloyd-Puryear, M.A.3
-
3
-
-
36048931014
-
Council on Children with Disabilities. Identification and evaluation of children with autism spectrum disorders
-
Johnson C.P., and Myers S.M. Council on Children with Disabilities. Identification and evaluation of children with autism spectrum disorders. Pediatrics 120 (2007) 1183-1215
-
(2007)
Pediatrics
, vol.120
, pp. 1183-1215
-
-
Johnson, C.P.1
Myers, S.M.2
-
4
-
-
38749141432
-
A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the Fragile X (FMR1) gene in newborn and high-risk populations
-
Tassone F., Pan R., Amiri K., et al. A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the Fragile X (FMR1) gene in newborn and high-risk populations. J Mol Diagn 10 (2008) 43-49
-
(2008)
J Mol Diagn
, vol.10
, pp. 43-49
-
-
Tassone, F.1
Pan, R.2
Amiri, K.3
-
5
-
-
52249117609
-
Supporting family adaptation to presymptomatic and "untreatable" conditions in an era of expanded newborn screening
-
Available at:, Accessed August 20, 2008
-
Bailey DB, Armstrong FD, Kemper AR, et al. Supporting family adaptation to presymptomatic and "untreatable" conditions in an era of expanded newborn screening. J Pediatr Psychol. 2008:1-14. Available at: http://jpepsy.oxfordjournals.org/cgi/content/abstract/jsn032. Accessed August 20, 2008.
-
(2008)
J Pediatr Psychol
, pp. 1-14
-
-
Bailey, D.B.1
Armstrong, F.D.2
Kemper, A.R.3
et al4
-
6
-
-
40949109764
-
Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues
-
Bailey D.B., Skinner D., Davis A.M., et al. Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues. Pediatrics 121 (2008) e693-e704
-
(2008)
Pediatrics
, vol.121
-
-
Bailey, D.B.1
Skinner, D.2
Davis, A.M.3
-
7
-
-
27644437938
-
Newborn screening for developmental disabilities: reframing presumptive benefit
-
Bailey D.B., Skinner D., and Warren S.F. Newborn screening for developmental disabilities: reframing presumptive benefit. Am J Public Health 95 (2005) 1889-1893
-
(2005)
Am J Public Health
, vol.95
, pp. 1889-1893
-
-
Bailey, D.B.1
Skinner, D.2
Warren, S.F.3
-
8
-
-
0035746538
-
FMR1 and the fragile X syndrome: human genome epidemiology review
-
Crawford D., Acuna J.M., and Sherman S.L. FMR1 and the fragile X syndrome: human genome epidemiology review. Genet Med 3 (2001) 359-371
-
(2001)
Genet Med
, vol.3
, pp. 359-371
-
-
Crawford, D.1
Acuna, J.M.2
Sherman, S.L.3
-
9
-
-
0142031147
-
Screening for Fragile X Syndrome: parent attitudes and perspectives
-
Skinner D., Sparkman K.L., and Bailey D.B. Screening for Fragile X Syndrome: parent attitudes and perspectives. Genet Med 5 (2003) 378-384
-
(2003)
Genet Med
, vol.5
, pp. 378-384
-
-
Skinner, D.1
Sparkman, K.L.2
Bailey, D.B.3
-
10
-
-
33644665924
-
Pediatricians' attitudes toward expanding newborn screening
-
Acharya K., Ackerman P.D., and Ross L.F. Pediatricians' attitudes toward expanding newborn screening. Pediatrics 116 (2005) e476-e484
-
(2005)
Pediatrics
, vol.116
-
-
Acharya, K.1
Ackerman, P.D.2
Ross, L.F.3
-
11
-
-
33645419803
-
Attitudes toward prenatal screening and testing for Fragile X
-
Fanos J.H., Spanger K.A., and Musci T.J. Attitudes toward prenatal screening and testing for Fragile X. Genet Med 8 (2006) 129-133
-
(2006)
Genet Med
, vol.8
, pp. 129-133
-
-
Fanos, J.H.1
Spanger, K.A.2
Musci, T.J.3
|