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Francesco Brancati

Showing results (1-10 of 155) with videos related to

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European Journal of Human Genetics : EJHG|September 26, 2003
Recurrent triploidy of maternal originFrancesco Brancati, Rita Mingarelli, Bruno Dallapiccola
Orphanet Journal of Rare Diseases|December 14, 2006
KBG syndromeFrancesco Brancati, Anna Sarkozy, Bruno Dallapiccola
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 7, 2015
Neurodevelopmental attributes of joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type: Update and perspectivesGiulia Ghibellini, Francesco Brancati, Marco Castori
Orphanet Journal of Rare Diseases|July 10, 2010
Joubert Syndrome and related disordersFrancesco Brancati, Bruno Dallapiccola, Enza Maria Valente
European Journal of Medical Genetics|January 1, 2008
Genotypes and phenotypes of Joubert syndrome and related disordersEnza Maria Valente, Francesco Brancati, Bruno Dallapiccola
Journal of Genetic Counseling|April 30, 2025
Perceived cancer risk and genetic counseling: A biopsychological perspectiveEleonora Cilli, Francesco Brancati, Dina Di Giacomo
American Journal of Medical Genetics. Part A|November 10, 2005
Majewski osteodysplastic primordial dwarfism type II (MOPD II) complicated by stroke: clinical report and review of cerebral vascular anomaliesFrancesco Brancati, Marco Castori, Rita Mingarelli, et al.
American Journal of Medical Genetics|September 5, 2002
Primary hypothyroidism and osteopenia associated with Neuhauser syndromeAnna Sarkozy, Rita Mingarelli, Francesco Brancati, et al.
American Journal of Medical Genetics. Part A|April 23, 2004
Ablepharon-macrostomia syndrome in a 46-year-old womanFrancesco Brancati, Rita Mingarelli, Anna Sarkozy, et al.
Pediatric Radiology|January 25, 2006
HypochondrogenesisMarco Castori, Francesco Brancati, Alessandro Castriota Scanderbeg, et al.
Pageof 16

Showing results (1-10 of 155) with videos related to

Sort By:
Pageof 16
European Journal of Human Genetics : EJHG|September 26, 2003
Recurrent triploidy of maternal originFrancesco Brancati, Rita Mingarelli, Bruno Dallapiccola
Orphanet Journal of Rare Diseases|December 14, 2006
KBG syndromeFrancesco Brancati, Anna Sarkozy, Bruno Dallapiccola
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 7, 2015
Neurodevelopmental attributes of joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type: Update and perspectivesGiulia Ghibellini, Francesco Brancati, Marco Castori
Orphanet Journal of Rare Diseases|July 10, 2010
Joubert Syndrome and related disordersFrancesco Brancati, Bruno Dallapiccola, Enza Maria Valente
European Journal of Medical Genetics|January 1, 2008
Genotypes and phenotypes of Joubert syndrome and related disordersEnza Maria Valente, Francesco Brancati, Bruno Dallapiccola
Journal of Genetic Counseling|April 30, 2025
Perceived cancer risk and genetic counseling: A biopsychological perspectiveEleonora Cilli, Francesco Brancati, Dina Di Giacomo
American Journal of Medical Genetics. Part A|November 10, 2005
Majewski osteodysplastic primordial dwarfism type II (MOPD II) complicated by stroke: clinical report and review of cerebral vascular anomaliesFrancesco Brancati, Marco Castori, Rita Mingarelli, et al.
American Journal of Medical Genetics|September 5, 2002
Primary hypothyroidism and osteopenia associated with Neuhauser syndromeAnna Sarkozy, Rita Mingarelli, Francesco Brancati, et al.
American Journal of Medical Genetics. Part A|April 23, 2004
Ablepharon-macrostomia syndrome in a 46-year-old womanFrancesco Brancati, Rita Mingarelli, Anna Sarkozy, et al.
Pediatric Radiology|January 25, 2006
HypochondrogenesisMarco Castori, Francesco Brancati, Alessandro Castriota Scanderbeg, et al.
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