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F Gurrieri

Showing results (11-20 of 37) with videos related to

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American Journal of Medical Genetics|October 2, 2001
Rearrangements of chromosome 15 in epilepsyL Torrisi, E Sangiorgi, L Russo, 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 Human Genetics|October 1, 1994
Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneityF Gurrieri, M Genuardi, P Chiurazzi, 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.
FEBS Letters|September 15, 2001
Genomic organization and embryonic expression of Suppressor of Fused, a candidate gene for the split-hand/split-foot malformation type 3T Grimm, S Teglund, D Tackels, et al.
American Journal of Medical Genetics|January 10, 1997
FISH characterization of small supernumerary marker chromosomes in two Prader-Willi patientsD Bettio, N Rizzi, D Giardino, et al.
Lupus|November 9, 2016
An autosomal recessive DNASE1L3-related autoimmune disease with unusual clinical presentation mimicking systemic lupus erythematosusA Carbonella, G Mancano, E Gremese, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|October 2, 2001
Rearrangements of chromosome 15 in epilepsyL Torrisi, E Sangiorgi, L Russo, 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 Human Genetics|October 1, 1994
Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneityF Gurrieri, M Genuardi, P Chiurazzi, 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.
FEBS Letters|September 15, 2001
Genomic organization and embryonic expression of Suppressor of Fused, a candidate gene for the split-hand/split-foot malformation type 3T Grimm, S Teglund, D Tackels, et al.
American Journal of Medical Genetics|January 10, 1997
FISH characterization of small supernumerary marker chromosomes in two Prader-Willi patientsD Bettio, N Rizzi, D Giardino, et al.
Lupus|November 9, 2016
An autosomal recessive DNASE1L3-related autoimmune disease with unusual clinical presentation mimicking systemic lupus erythematosusA Carbonella, G Mancano, E Gremese, et al.
Pageof 4