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Gross and fine motor development in 45,X and 47,XXX girls.

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Prenatal diagnosis and management of sex chromosome aneuploidy:

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Taurodontism in females with extra X chromosomes.

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Prediction of an abnormal karyotype in fetuses with omphalocele Prenat.

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Twenty-one propositae 8 to 19 years of age, identified through newborn screening to be 45,X, 47,XXX, or 45,X mosaic, and 11 control girls were evaluated by a physical therapist unaware of their genetic constitution.

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Sex chromosome mosaics were more similar to control girls.

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Speech and language development in 41 children with sex chromosome anomalies.

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Klinefelter and Trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15 - a coincidence?

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