41 Infos zu Helen Fryssira

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1 Aktuelle Nachrichten

4 Profile in Sozialen Netzwerken

LinkedIn: Helen Fryssira - Ass. Professor in Medical Genetics - University of ...

View Helen Fryssira's profile on LinkedIn, the world's largest professional community. Helen has 1 job listed on their profile. See the complete profile on LinkedIn ...

LinkedIn: Helen Fryssira | LinkedIn

Sehen Sie sich das Profil von Helen Fryssira auf LinkedIn an, dem weltweit größten beruflichen Netzwerk. Helen Fryssira hat 1 Job im Profil angegeben. Sehen ...

Fryssira Helen | Semantic Scholar

Semantic Scholar profile for ,, with 3 scientific research papers.

Loop | Helen Fryssira

Agia Sophia Children's Hospital. Athens, Greece. Primary. View All. mini profile avatar Helen Fryssira. Overview · Bio · Network · Publications · Editorial ...

1 Hobbys & Interessen

Clinical, genetic and cellular analysis of forty-nine osteopetrotic...

... Claudio Letizia PubMed articlesGoogle scholar articles; Gabriella Bianchini PubMed articlesGoogle scholar articles; Helen Fryssira PubMed ...

1 Persönliche Webseiten

Triple-X syndroom - Internationa(a)l Triple-X Contact/Support Groups

To Mellon-Association of people with genetic disorders. Dr. Helen Fryssira Medical genetics, University of Athens, Aghia Sophia Children's hospital. Makrinitsas ...

4 Bücher zum Namen

Helen Fryssira | Hilaris SRL

Helen Fryssira, Human Genetics & Embryology

Gentaur antibody-antibodies.com The Marketplace for Antibodies :

antibody-antibodies.com is the marketplace for research antibodies. Find the right antibody for your research needs.

Central precocious puberty in a boy with 22q13 deletion syndrome and...

Helen Fryssira and Maria Tzetis: Department of Medical Genetics, ... Aris Giannakopoulos*, Helen Fryssira, Maria Tzetis, Athina Xaidara.

Growth Hormone Deficiency in a Child with Williams-Beuren Syndrome....

Paraskevi Xekouki, / Helen Fryssira, / Maria Maniati-Christidi, / Styliani Amenta, / Emmanouel M. Karavitakis, / Christina Kanaka-Gantenbein, ...

5 Dokumente

Helen Fryssira - Academia.edu

Academia.edu is a place to share and follow research.

Cranioectodermal dysplasia: A probable ciliopathy - [PDF Document]

CLINICAL REPORT Cranioectodermal Dysplasia: A Probable Ciliopathy Anastasia E. Konstantinidou,1* Helen Fryssira,2 Stavros Sifakis,3 Charalampos Karadimas,4...

EBSCOhost | | Constitutional and somatic deletions of the...

Helen Fryssira (). Laurent Bermont (laurent.bermont@univ- fcomte.fr). Christophe Ferrand (.fr).

Tumor development in three patients with Noonan syndrome

ORIGINAL PAPER Tumor development in three patients with Noonan syndrome Helen Fryssira & George Leventopoulos & Stavroula Psoni & Sophia Kitsiou-Tzeli &...

2 Wissenschaftliche Publikationen

Bone Marrow Failure in Fanconi Anemia: Clinical and Genetic Spect...:...

Helen Fryssira, MD, PhD,‡ and Sophia Polychronopoulou, MD, PhD*. Summary: Prognostic refinement in Fanconi anemia (FA) is needed, especially when ...

Erratum to: An interstitial deletion at 8q23.1-q associated with...

Nikoletta SelentiEmail author,; Maria Tzetis,; Maria Braoudaki,; Krinio Giannikou,; Sofia Kitsiou-Tzeli and; Helen Fryssira. Molecular Cytogenetics20158:73.

2 Allgemeine Veröffentlichungen

A novel large deletion of the ICR1 region including H19 and …tive...

Helen Fryssira Email author; Stella Amenta; Deniz Kanber; Christalena Sofocleous; Evangelia Lykopoulou; Christina Kanaka-Gantenbein ...

Erratum to: An interstitial deletion at 8q23.1-q associated with...

Maria Tzetis; Maria Braoudaki; Krinio Giannikou; Sofia Kitsiou-Tzeli; Helen Fryssira. Nikoletta Selenti. 1. Email author; Maria Tzetis. 1.

1 Meinungen & Artikel

Phenotypic and Genotypic Variability in Four Males With MECP2 Gene...

Clinical Investigation

21 Webfunde aus dem Netz

‪HELEN FRYSSIRA‬ - ‪Μελετητής Google‬

‪PROF‬ - ‪‪Παρατίθεται από ‬‬ - ‪CLINICAL GENETICS‬

Helen Fryssira: free download. Ebooks library. On-line books store on...

Helen Fryssira: free download. Ebooks library. On-line books store on Z-Library | Z-Library. Download books for free. Find books

Orphanet: Pr Helen FRYSSIRA

The portal for rare diseases and orphan drugs

(PDF) Noonan syndrome: a report of 2 paediatric cases | Helen...

Konstantina 1 Vavetsi , Panagiotis 1 Koromantzos , Dimitris Emmanouil 2, Yiorgos 1 Bobetsis , 3 Helen Fryssira , Phoebus Madianos 1 1Department of ...

Clinical spectrum of females with HCCS mutation: from no clinical...

Vanessa van Rahden 1 Isabella Rau 1 Sigrid Fuchs 1 Friederike Kosyna 1 Hiram de Almeida 2Helen Fryssira 3 Bertrand Isidor 4, 5 Anna Jauch 6 Madeleine ...

Items where Division is "Faculties (pre reorg) > Faculty of...

Nonverbal communication, play, and language in Greek young children with Williams syndrome - Christina F. Papaeliou, Helen Fryssira, Anastassios Kodakos, ...

JNS Vol 395 | December 2018

Journal of the Neurological Sciences Vol 395 | 15 December | Pages

A Clinical Study of Sotos Syndrome Patients With Review of the...

... of the Literature. George Leventopoulos, Sophia Kitsiou-Tzeli, Konstantinos Kritikos, Stavroula Psoni, Ariadni Mavrou, Emmanuel Kanavakis, Helen Fryssira.

Diagnostic exome sequencing to elucidate the genetic basis ...

... Stavroula Psoni, Sofia Kitsiou-Tzeli, Helen Fryssira, Emmanouil Kanavakis, Nasir Al-Allawi, Abdelaziz Sefiani, Sana' Al Hait, Siham C Elalaoui, Nadine Jalkh,  ...

Further delineation of novel 1p36 rearrangements by array-CGH...

Krinio Giannikou , Helen Fryssira , Vasilis Oikonomakis , Areti Syrmou , Konstantina Kosma , Maria Tzetis , Sofia Kitsiou-Tzeli , Emmanouel Kanavakis.

Lack of IL7Rα expression in T cells is a hallmark of T-cell...

... Katie Felix, Christy Mayfield, Benjamin Dekel, Arend Bokenkamp, Helen Fryssira, Encarna Guillen-Navarro, Giuliana Lama, Milena Brugnara, ...

Rothmund-Thomson Syndrome - Research - Aarhus University

author = "Aude-Annick Suter and Peter Itin and Karl Heinimann and Munaza Ahmed and Tazeen Ashraf and Helen Fryssira and Usha Kini and Pablo Lapunzina ...

Nonverbal communication, play, and language in Greek young children...

Author: Helen Fryssira. Author: Anastassios Kodakos. Author: Maria Kaila. Author : Evangelia Benaveli. Author: Konstantinos Michaelides. Author: Vassilis ...

Schimke immunoosseous dysplasia: Suggestions of genetic diversity...

J. Marietta Clewing, Helen Fryssira, David Goodman, Sarah F. Smithson, Emily A. Sloan, Shu Lou, Yan Huang, Kunho Choi, Thomas Lücke, Harika Alpay, Jean ...

OPUS FAU | Clinical spectrum of females with HCCS mutation: from no...

Vanessa A. van Rahden, Isabella Rau, Sigrid Fuchs, Friederike K. Kosyna, Hiram Larangeira de Almeida, Helen Fryssira, Bertrand Isidor, Anna ...

Pachyonychia Congenita - Patient Associations :: Geneskin

TO MELLON - Association of people with genetic disorders. Makrinitsas 16, Abelokipoi ATHENS GREECE Dr Helen FRYSSIRA . gr ...

δημοσιεύσεις, εργασίες | Psychiatriki

Άρθρα-Δημοσιεύσεις-Συγγραφικό έργο: • “COMT and MTHFR polymorphisms interaction on cognition in schizophrenia: An exploratory study”. Dimitrios Kontis, Eirini...

Reduced elastogenesis: A clue to the arteriosclerosis and...

... Georges Deschenes, M. Semin Fenkçi, Pierre Frange, Stefan Fründ, Helen Fryssira, Encarna Guillen-Navarro, Kory Keller, Salman Kirmani, Christine Kobelka ...

Frequent COL4 mutations in familial microhematuria accompanied by...

The author haven't finished explaining this publication. Read Publication. The following have contributed to this page: Professor Helen Fryssira. PDF generated  ...

Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange...

...

Bedeutung zum Vornamen Helen

Weiblicher Vorname (Englisch): Helen; die Strahlende; Altgriechisch (Griechische Mythologie); helene = die Fackel, der Glanz, die Sonnenstrahlen; in der griechischen Mythology ist Helena die Tochter von Zeus und Leda; ihre Entführung war der Grund für den Trojanischen Krieg; der Name 'Helios' des griechischen Sonnengotts hat dieselben Wurzeln

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