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Helen Fryssira

Showing results (1-10 of 43) with videos related to

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Molecular Genetics & Genomic Medicine|October 6, 2015
Medical genetics and genomic medicine in Greece: achievements and challengesIrini Manoli, Helen Fryssira
Clinical Pediatrics|March 10, 2006
PHACE syndrome: a new caseHelen Fryssira, Artemis Tsitsika, Athanassia Lourida, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Growth hormone deficiency in a case of cerebrofaciothoracic syndrome in one of two affected siblingsChristina Kanaka-Gantenbein, Helen Fryssira, George Chrousos, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 29, 2016
Central precocious puberty in a boy with 22q13 deletion syndrome and NOTCH-1 gene duplicationAris Giannakopoulos, Helen Fryssira, Maria Tzetis, et al.
Cancer Genetics and Cytogenetics|September 24, 2004
Non-Hodgkin lymphoma in a child with Williams syndromeStyliani Amenta, Maria Moschovi, Christalena Sofocleous, et al.
Molecular Cytogenetics|August 14, 2015
An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4Nikoletta Selenti, Maria Tzetis, Maria Braoudaki, et al.
Molecular Cytogenetics|October 3, 2015
Erratum to: An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4Nikoletta Selenti, Maria Tzetis, Maria Braoudaki, et al.
Clinical Dysmorphology|October 29, 2002
A male with polysyndactyly, linear skin defects and sclerocornea. Goltz syndrome versus MIDASHelen Fryssira, Miltiadis Papathanassiou, Joanna Barbounaki, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 1, 2010
Incontinentia pigmenti revisited. A novel nonsense mutation of the IKBKG geneHelen Fryssira, Talia Kakourou, Manthoula Valari, et al.
European Journal of Pediatrics|December 7, 2007
Tumor development in three patients with Noonan syndromeHelen Fryssira, George Leventopoulos, Stavroula Psoni, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Molecular Genetics & Genomic Medicine|October 6, 2015
Medical genetics and genomic medicine in Greece: achievements and challengesIrini Manoli, Helen Fryssira
Clinical Pediatrics|March 10, 2006
PHACE syndrome: a new caseHelen Fryssira, Artemis Tsitsika, Athanassia Lourida, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Growth hormone deficiency in a case of cerebrofaciothoracic syndrome in one of two affected siblingsChristina Kanaka-Gantenbein, Helen Fryssira, George Chrousos, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 29, 2016
Central precocious puberty in a boy with 22q13 deletion syndrome and NOTCH-1 gene duplicationAris Giannakopoulos, Helen Fryssira, Maria Tzetis, et al.
Cancer Genetics and Cytogenetics|September 24, 2004
Non-Hodgkin lymphoma in a child with Williams syndromeStyliani Amenta, Maria Moschovi, Christalena Sofocleous, et al.
Molecular Cytogenetics|August 14, 2015
An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4Nikoletta Selenti, Maria Tzetis, Maria Braoudaki, et al.
Molecular Cytogenetics|October 3, 2015
Erratum to: An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4Nikoletta Selenti, Maria Tzetis, Maria Braoudaki, et al.
Clinical Dysmorphology|October 29, 2002
A male with polysyndactyly, linear skin defects and sclerocornea. Goltz syndrome versus MIDASHelen Fryssira, Miltiadis Papathanassiou, Joanna Barbounaki, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 1, 2010
Incontinentia pigmenti revisited. A novel nonsense mutation of the IKBKG geneHelen Fryssira, Talia Kakourou, Manthoula Valari, et al.
European Journal of Pediatrics|December 7, 2007
Tumor development in three patients with Noonan syndromeHelen Fryssira, George Leventopoulos, Stavroula Psoni, et al.
Pageof 5