Multisystem study of 20 older adults with Williams syndrome von Cherniske, Elizabeth M., Carpenter, Thomas O., Klaiman, Cheryl, Young, Eytan, Bregman, Joel, Insogna, Karl, Schultz, Robert T., Pober, Barbara R.

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Truncating mutations in FOXC2 cause multiple lymphedema syndromes von FINEGOLD, David N, KIMAK, Mark A, LAWRENCE, Elizabeth C, LEVINSON, Kara L, CHERNISKE, Elizabeth M, POBER, Barbara R, DUNLAP, Jean W, FERRELL, Robert E

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Hearing from parents: The impact of receiving the diagnosis of Williams syndrome in their child von Waxler, Jessica L., Cherniske, Elizabeth M., Dieter, Kristen, Herd, Pamela, Pober, Barbara R.

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46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters von Hisama, Fuki M., Zemel, Sharon, Cherniske, Elizabeth M., Vladutiu, Georgirene D., Pober, Barbara R.

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Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis : a new X linked contiguous gene deletion syndrome? von JONSSON, J. J, RENIERI, A, GALLAGHER, P. G, KASHTAN, C. E, CHERNISKE, E. M, BRUTTINI, M, PICCINI, M, VITELLI, F, BALLABIO, A, POBER, B. R

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Early puberty in Williams syndrome von Cherniske, E M, Sadler, L S, Schwartz, D, Carpenter, T O, Pober, B R

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