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Nancy J. Carpenter

University of Oklahoma

37

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920

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The course of cognitive-behavioral development in children with the FMR1 mutation, Williams–Beuren syndrome, and neurofibromatosis type 1: The effect of gender†

2010 American Journal of Medical Genetics Part A
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Down syndrome due to 21;21 translocation in a male twin.

2008 Clinical Genetics
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Studies of age‐correlated features of cognitive‐behavioral development in children and adolescents with genetic disorders

2007 American Journal of Medical Genetics Part A
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Mutations of ARX are associated with striking pleiotropy and consistent genotype–phenotype correlation

2004 Human Mutation
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Age-related language characteristics of children and adolescents with fragile X syndrome.

1999 American Journal of Medical Genetics
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Prenatal Diagnosis of Monosomy 6 and Ring Chromosome 6 in a Fetus with Ventriculomegaly

1999 Pediatric Research
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X-linked mental retardation syndrome with characteristic coarse facial appearance, brachydactyly, and short stature maps to proximal Xq

1999 American Journal of Medical Genetics
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Regional localization of a nonspecific X‐linked mental retardation gene (MRX59) to Xp21.2‐p22.2

1999 American Journal of Medical Genetics
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Refined gene localization for the Miles‐Carpenter syndrome (MCS)

1999 American Journal of Medical Genetics
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Rater reliability of fragile X mutation size estimates: A multilaboratory analysis

1996 American Journal of Medical Genetics
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Citations (8)