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European Journal of Human Genetics : EJHG
|
September 26, 2003
Recurrent triploidy of maternal origin
Francesco Brancati, Rita Mingarelli, Bruno Dallapiccola
Orphanet Journal of Rare Diseases
|
December 14, 2006
KBG syndrome
Francesco 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 perspectives
Giulia Ghibellini, Francesco Brancati, Marco Castori
Orphanet Journal of Rare Diseases
|
July 10, 2010
Joubert Syndrome and related disorders
Francesco Brancati, Bruno Dallapiccola, Enza Maria Valente
European Journal of Medical Genetics
|
January 1, 2008
Genotypes and phenotypes of Joubert syndrome and related disorders
Enza Maria Valente, Francesco Brancati, Bruno Dallapiccola
Journal of Genetic Counseling
|
April 30, 2025
Perceived cancer risk and genetic counseling: A biopsychological perspective
Eleonora 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 anomalies
Francesco Brancati, Marco Castori, Rita Mingarelli, et al.
American Journal of Medical Genetics
|
September 5, 2002
Primary hypothyroidism and osteopenia associated with Neuhauser syndrome
Anna 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 woman
Francesco Brancati, Rita Mingarelli, Anna Sarkozy, et al.
Pediatric Radiology
|
January 25, 2006
Hypochondrogenesis
Marco Castori, Francesco Brancati, Alessandro Castriota Scanderbeg, et al.
Page
of 16
Search research articles
Search
Showing results (1-10 of 155) with videos related to
Sort By:
Page
of 16
European Journal of Human Genetics : EJHG
|
September 26, 2003
Recurrent triploidy of maternal origin
Francesco Brancati, Rita Mingarelli, Bruno Dallapiccola
Orphanet Journal of Rare Diseases
|
December 14, 2006
KBG syndrome
Francesco 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 perspectives
Giulia Ghibellini, Francesco Brancati, Marco Castori
Orphanet Journal of Rare Diseases
|
July 10, 2010
Joubert Syndrome and related disorders
Francesco Brancati, Bruno Dallapiccola, Enza Maria Valente
European Journal of Medical Genetics
|
January 1, 2008
Genotypes and phenotypes of Joubert syndrome and related disorders
Enza Maria Valente, Francesco Brancati, Bruno Dallapiccola
Journal of Genetic Counseling
|
April 30, 2025
Perceived cancer risk and genetic counseling: A biopsychological perspective
Eleonora 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 anomalies
Francesco Brancati, Marco Castori, Rita Mingarelli, et al.
American Journal of Medical Genetics
|
September 5, 2002
Primary hypothyroidism and osteopenia associated with Neuhauser syndrome
Anna 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 woman
Francesco Brancati, Rita Mingarelli, Anna Sarkozy, et al.
Pediatric Radiology
|
January 25, 2006
Hypochondrogenesis
Marco Castori, Francesco Brancati, Alessandro Castriota Scanderbeg, et al.
Page
of 16