Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS
Mendoza-Londono, Roberto, Lammer, Edward, Watson, Rosemarie, Harper, John, Hatamochi, Atsushi, Hatamochi-Hayashi, Saori, Napierala, Dobrawa, Hermanns, Pia, Collins, Sinead, Roa, Benjamin B., Hedge, Madhuri R., Wakui, Keiko, Nguyen, Diep, Stockton, David W., Lee, Brendan
Published in American journal of human genetics (01.07.2005)
Published in American journal of human genetics (01.07.2005)
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Limb girdle muscular dystrophy: use of dHPLC and direct sequencing to detect sarcoglycan gene mutations in a New Zealand cohort
HEDGE, M. R, WU, F, CHONG, B, CHIN, E. L. H, HUTCHINSON, D. O, RICHARDS, C. S, KHADILKAR, S, LOVE, D. R
Published in Clinical genetics (01.01.2004)
Published in Clinical genetics (01.01.2004)
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Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standards
Williams, LC, Hedge, MR, Herrera, G, Stapleton, PM, Love, DR
Published in Molecular and cellular probes (01.08.1999)
Published in Molecular and cellular probes (01.08.1999)
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