A
Anna Calabro
Researcher at University of Perugia
Publications - 20
Citations - 282
Anna Calabro is an academic researcher from University of Perugia. The author has contributed to research in topics: Anophthalmia & Dermatoglyphics. The author has an hindex of 9, co-authored 20 publications receiving 278 citations. Previous affiliations of Anna Calabro include Catholic University of the Sacred Heart.
Papers
More filters
Journal ArticleDOI
Omphalocele and gastroschisis: a collaborative study of five Italian congenital malformation registries.
Elisa Calzolari,S. Volpato,Fabrizio Bianchi,Cianciulli D,Romano Tenconi,Maurizio Clementi,Anna Calabro,S. Lungarotti,Pierpaolo Mastroiacovo,Lorenzo D. Botto,Amedeo Spagnolo,Mario Milan +11 more
TL;DR: During 1984-1989, 116 cases of omphalocele and 42 cases of gastroschisis were detected among 736,760 consecutive births in the area covered by five Italian congenital malformation registries.
Journal ArticleDOI
Anophthalmia and benomyl in Italy: a multicenter study based on 940,615 newborns
Amedeo Spagnolo,Fabrizio Bianchi,Anna Calabro,Elisa Calzolari,Maurizio Clementi,Peirpaolo Mastroiacovo,Paola Meli,G. Petrelli,Romano Tenconi +8 more
TL;DR: An association between Benomyl use and congenital micro/anophthalmia appears to be unlikely, though the limits intrinsic to ecologic correlation studies must be taken into account.
Journal ArticleDOI
Fibrochondrogenesis: radiologic and histologic studies.
Donna Jane Eteson,Gerald E. Adomian,Asher Ornoy,Toshio Koide,Yasuo Sugiura,Anna Calabro,Serena Lungarotti,Pierpaolo Mastroiacovo,Ralph S. Lachman,David L. Rimoin +9 more
TL;DR: Fibrochondrogenesis is a distinct, neonatally lethal, short-limb skeletal dysplasia which was first described in a single patient in 1978 and now has distinct radiographic and chondro-osseous morphologic defects different from those seen in the other known skeletal Dysplasias.
Journal ArticleDOI
De novo duplication 1q32-q42: variability of phenotypic features in partial lq trisomics.
TL;DR: It is concluded that, at present, it is impossible to delineate the profile of the syndromes resulting from partial 1q trisomies.
Journal ArticleDOI
Interstitial deletion 13q syndromes: a report on two unrelated patients.
M. Serena-Lungarotti,Anna Calabro,G. Mariotti,Pierpaolo Mastroiacovo,Silvana Provenzano,Bruno Dallapiccola +5 more
TL;DR: The karyotype-phenotype correlation in the two patients suggests the need to reconsider the clinical profile of these rare chromosomal syndromes in a large series of subjects.