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American Journal of Medical Genetics|September 15, 1992
Further delineation of the Simpson-Golabi-Behmel (SGB) syndromeF Gurrieri, M Cappa, G NeriAmerican Journal of Medical Genetics|October 22, 1998
Clinical and molecular aspects of the Simpson-Golabi-Behmel syndromeG Neri, F Gurrieri, G Zanni, et al.American Journal of Medical Genetics|May 5, 2001
New syndrome of mental retardation, Robin sequence, and brachydactylyF Gurrieri, K Steindl, S Giglio, et al.American Journal of Medical Genetics|February 1, 1991
XLMR genes: update 1990G Neri, F Gurrieri, A Gal, et al.American Journal of Medical Genetics|April 1, 1992
Possible new type of oral-facial-digital syndrome with retinal abnormalities: OFDS type (VIII)F Gurrieri, V Sammito, B Ricci, et al.American Journal of Medical Genetics|May 1, 1994
Gene for Simpson-Golabi-Behmel syndrome is linked to HPRT in Xq26 in two European familiesU Orth, F Gurrieri, A Behmel, et al.Neurology|May 20, 1999
Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13F Gurrieri, A Battaglia, L Torrisi, et al.American Journal of Medical Genetics|January 30, 1995
Ulnar ray defect in an infant with a 6q21;7q31.2 translocation: further evidence for the existence of a limb defect gene in 6q21F Gurrieri, M Cammarata, R M Avarello, et al.American Journal of Medical Genetics. Part A|January 5, 2011
The Simpson-Golabi-Behmel syndrome: A clinical case and a detective storyF Gurrieri, M G Pomponi, R Pietrobono, et al.Pageof 49