TY  - GEN
AU  - Abrams,Liane
AU  - Cronister,Amy
AU  - Brown,William T
AU  - Tassone,Flora
AU  - Sherman,Stephanie L
AU  - Finucane,Brenda
AU  - McConkie-Rosell,Allyn
AU  - Hagerman,Randi
AU  - Kaufmann,Walter E
AU  - Picker,Jonathan
AU  - Coffey,Sarah
AU  - Skinner,Debra
AU  - Johnson,Vanessa
AU  - Miller,Robert
AU  - Berry-Kravis,Elizabeth
TI  - Newborn, carrier, and early childhood screening recommendations for fragile X
SN  - 1098-4275
PY  - 2013///0204
KW  - Adolescent
KW  - Adult
KW  - Alleles
KW  - Animals
KW  - Ataxia
KW  - diagnosis
KW  - Attention Deficit Disorder with Hyperactivity
KW  - Autistic Disorder
KW  - Child
KW  - Child, Preschool
KW  - Cooperative Behavior
KW  - DNA Mutational Analysis
KW  - Early Diagnosis
KW  - Female
KW  - Fragile X Mental Retardation Protein
KW  - genetics
KW  - Fragile X Syndrome
KW  - Genetic Carrier Screening
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Interdisciplinary Communication
KW  - Male
KW  - Mice
KW  - Mice, Knockout
KW  - Models, Genetic
KW  - Neonatal Screening
KW  - Patient Care Team
KW  - Polymerase Chain Reaction
KW  - Primary Ovarian Insufficiency
KW  - Referral and Consultation
KW  - Sex Factors
KW  - Tremor
KW  - Trinucleotide Repeats
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review
UR  - https://doi.org/10.1542/peds.2012-0693
ER  -