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    Results: 1 to 20 of 58

    1.

    Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

    Coffee B, Keith K, Albizua I, Malone T, Mowrey J, Sherman SL, Warren ST.

    Am J Hum Genet. 2009 Oct;85(4):503-14.PMID: 19804849 [PubMed - indexed for MEDLINE]Related articles

    2.

    Fragile X gene stability in Basque Valleys: prevalence of premutation and intermediate alleles.

    Arrieta I, Télez M, Huerta I, Flores P, Criado B, Ramírez JM, Barasoain M, Gónzalez AJ.

    Hum Biol. 2008 Dec;80(6):593-600.PMID: 19728537 [PubMed - indexed for MEDLINE]Related articles

    3.

    Using percentile schedules to increase eye contact in children with Fragile X syndrome.

    Hall SS, Maynes NP, Reiss AL.

    J Appl Behav Anal. 2009 Spring;42(1):171-6.PMID: 19721738 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Direct magnitude estimation of articulation rate in boys with fragile X syndrome.

    Zajac DJ, Harris AA, Roberts JE, Martin GE.

    J Speech Lang Hear Res. 2009 Oct;52(5):1370-9. Epub 2009 Aug 28.PMID: 19717654 [PubMed - indexed for MEDLINE]Related articles

    5.

    Functional skills of individuals with fragile x syndrome: a lifespan cross-sectional analysis.

    Bailey DB, Raspa M, Holiday D, Bishop E, Olmsted M.

    Am J Intellect Dev Disabil. 2009 Jul;114(4):289-303.PMID: 19642710 [PubMed - indexed for MEDLINE]Related articles

    6.

    Phonological accuracy and intelligibility in connected speech of boys with fragile X syndrome or Down syndrome.

    Barnes E, Roberts J, Long SH, Martin GE, Berni MC, Mandulak KC, Sideris J.

    J Speech Lang Hear Res. 2009 Aug;52(4):1048-61.PMID: 19641081 [PubMed - indexed for MEDLINE]Related articles

    7.

    Recognition and reduction of the impact of inheritable causes of ovarian failure.

    Oliver A, Awala AO, Skidmore C, Cahill DJ.

    J Obstet Gynaecol. 2009 Jul;29(5):445. No abstract available. PMID: 19603333 [PubMed - indexed for MEDLINE]Related articles

    8.

    No change in the age of diagnosis for fragile x syndrome: findings from a national parent survey.

    Bailey DB Jr, Raspa M, Bishop E, Holiday D.

    Pediatrics. 2009 Aug;124(2):527-33. Epub 2009 Jul 5.PMID: 19581269 [PubMed - indexed for MEDLINE]Related articles

    9.

    Fragile X syndrome.

    Hayes EW, Matalon R.

    Pediatrics. 2009 Aug;124(2):790-2. Epub 2009 Jul 5. No abstract available. PMID: 19581265 [PubMed - indexed for MEDLINE]Related articles

    10.

    Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India.

    Guruju MR, Lavanya K, Thelma BK, Sujatha M, OmSai VR, Nagarathna V, Amarjyothi P, Jyothi A, Anandaraj MP.

    J Clin Neurosci. 2009 Oct;16(10):1305-10. Epub 2009 Jun 27.PMID: 19560928 [PubMed - indexed for MEDLINE]Related articles

    11.

    Expansion of an FMR1 grey-zone allele to a full mutation in two generations.

    Fernandez-Carvajal I, Lopez Posadas B, Pan R, Raske C, Hagerman PJ, Tassone F.

    J Mol Diagn. 2009 Jul;11(4):306-10. Epub 2009 Jun 12.PMID: 19525339 [PubMed - indexed for MEDLINE]Related articles

    12.

    Polymerase chain reaction, nuclease digestion, and mass spectrometry based assay for the trinucleotide repeat status of the fragile X mental retardation 1 gene.

    Dodds ED, Tassone F, Hagerman PJ, Lebrilla CB.

    Anal Chem. 2009 Jul 1;81(13):5533-40.PMID: 19514725 [PubMed - indexed for MEDLINE]Related articles

    13.

    Discrimination of common and unique RNA-binding activities among Fragile X mental retardation protein paralogs.

    Darnell JC, Fraser CE, Mostovetsky O, Darnell RB.

    Hum Mol Genet. 2009 Sep 1;18(17):3164-77. Epub 2009 Jun 1.PMID: 19487368 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Delay eyeblink classical conditioning is impaired in Fragile X syndrome.

    Tobia MJ, Woodruff-Pak DS.

    Behav Neurosci. 2009 Jun;123(3):665-76.PMID: 19485573 [PubMed - indexed for MEDLINE]Related articles

    15.

    Levetiracetam improves intention tremor in fragile x-associated tremor/ataxia syndrome.

    Saponara R, Greco S, Proto G, Trubia T, Domina E.

    Clin Neuropharmacol. 2009 Jan-Feb;32(1):53-4.PMID: 19471185 [PubMed - indexed for MEDLINE]Related articles

    16.

    The role of DNA damage response pathways in chromosome fragility in Fragile X syndrome.

    Kumari D, Somma V, Nakamura AJ, Bonner WM, D'Ambrosio E, Usdin K.

    Nucleic Acids Res. 2009 Jul;37(13):4385-92. Epub 2009 May 21.PMID: 19465392 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population.

    Fernandez-Carvajal I, Walichiewicz P, Xiaosen X, Pan R, Hagerman PJ, Tassone F.

    J Mol Diagn. 2009 Jul;11(4):324-9. Epub 2009 May 21.PMID: 19460941 [PubMed - indexed for MEDLINE]Related articles

    18.

    You can build it ... but will they come?: the potential "expansion" of testing methodologies for fragile X syndrome.

    Potter NT.

    J Mol Diagn. 2009 Jul;11(4):279-80. Epub 2009 May 21. No abstract available. PMID: 19460939 [PubMed - indexed for MEDLINE]Related articles

    19.

    A quantitative ELISA assay for the fragile x mental retardation 1 protein.

    Iwahashi C, Tassone F, Hagerman RJ, Yasui D, Parrott G, Nguyen D, Mayeur G, Hagerman PJ.

    J Mol Diagn. 2009 Jul;11(4):281-9. Epub 2009 May 21.PMID: 19460937 [PubMed - indexed for MEDLINE]Related articles

    20.

    When to tell and test for genetic carrier status: perspectives of adolescents and young adults from fragile X families.

    Wehbe RM, Spiridigliozzi GA, Heise EM, Dawson DV, McConkie-Rosell A.

    Am J Med Genet A. 2009 Jun;149A(6):1190-9.PMID: 19449413 [PubMed - indexed for MEDLINE]Related articlesFree article

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