Abrams, Liane <br/><br/>
Newborn, carrier, and early childhood screening recommendations for fragile X.  [electronic resource] 

 -  Pediatrics  Dec 2012 
 - 1126-35 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review 
<br/><br/><label>ISSN: </label>1098-4275 
<br/><br/><label>Standard No.: </label>10.1542/peds.2012-0693  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alleles<br/>Animals<br/>Ataxia--diagnosis<br/>Attention Deficit Disorder with Hyperactivity--diagnosis<br/>Autistic Disorder--diagnosis<br/>Child<br/>Child, Preschool<br/>Cooperative Behavior<br/>DNA Mutational Analysis<br/>Early Diagnosis<br/>Female<br/>Fragile X Mental Retardation Protein--genetics<br/>Fragile X Syndrome--diagnosis<br/>Genetic Carrier Screening<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Interdisciplinary Communication<br/>Male<br/>Mice<br/>Mice, Knockout<br/>Models, Genetic<br/>Neonatal Screening<br/>Patient Care Team<br/>Polymerase Chain Reaction<br/>Primary Ovarian Insufficiency--diagnosis<br/>Referral and Consultation<br/>Sex Factors<br/>Tremor--diagnosis<br/>Trinucleotide Repeats--genetics