Search Results - Borrelli, P.
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Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis by Palka, Giandomenico (Author) , Stuppia, Liborio (Author) , Franchi, P. Guanciali (Author) , Chiarelli, F. (Author) , Fischetto, R. (Author) , Borrelli, P. (Author) , Giannotti, A. (Author) , Fioretti, G. (Author) , Rinaldi, Mm (Author) , Mingarelli, R. (Author) , Rappold, Gudrun (Author) , Calabrese, G. (Author) ,
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Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male by Stuppia, Liborio (Author) , Calabrese, Gaetano (Author) , Borrelli, P. (Author) , Gatta, V. (Author) , Morizio, E. (Author) , Mingarelli, R. (Author) , Di Gilio, M. C. (Author) , Crinò, A. (Author) , Giannotti, A. (Author) , Rappold, Gudrun (Author) , Palka, Giandomenico (Author) ,
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Related Subjects
Adolescent
Bone and Bones
DNA Mutational Analysis
Gene Deletion
Homeodomain Proteins
Humans
In Situ Hybridization, Fluorescence
Leri-Weill dyschondrosteosis
Male
Noonan Syndrome
Osteochondrodysplasias
Polymerase Chain Reaction
Radiography
SHOX
Short Stature Homeobox Protein
Turner syndrome
X Chromosome
haploinsufficiency