Newborn, carrier, and early childhood screening recommendations for fragile X. [electronic resource]
Producer: 20130204Description: 1126-35 p. digitalISSN:- 1098-4275
- Adolescent
- Adult
- Alleles
- Animals
- Ataxia -- diagnosis
- Attention Deficit Disorder with Hyperactivity -- diagnosis
- Autistic Disorder -- diagnosis
- Child
- Child, Preschool
- Cooperative Behavior
- DNA Mutational Analysis
- Early Diagnosis
- Female
- Fragile X Mental Retardation Protein -- genetics
- Fragile X Syndrome -- diagnosis
- Genetic Carrier Screening
- Genetic Predisposition to Disease -- genetics
- Humans
- Infant
- Infant, Newborn
- Interdisciplinary Communication
- Male
- Mice
- Mice, Knockout
- Models, Genetic
- Neonatal Screening
- Patient Care Team
- Polymerase Chain Reaction
- Primary Ovarian Insufficiency -- diagnosis
- Referral and Consultation
- Sex Factors
- Tremor -- diagnosis
- Trinucleotide Repeats -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review
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