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Search Results - Patsalis, Constantinos
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Investigating TNNC1 gene inheritance and clinical outcomes through a comprehensive familial study
by
Patsalis, Constantinos
,
Kyriakou, Skevi
,
Georgiadou, Michaella
,
Ioannou, Lygia
,
Constantinou, Louisa
,
Soteriou, Valando
,
Jossif, Antonis
,
Evangelidou, Paola
,
Sismani, Carolina
,
Kypri, Elena
,
Ioannides, Marios
,
Koumbaris, George
Published in
American journal of medical genetics. Part A
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Haploinsufficiency of the miR-873/miR-876 microRNA cluster is associated with craniofacial abnormalities
by
Koufaris, Costas
,
Papagregoriou, Gregoris
,
Kousoulidou, Ludmila
,
Moutafi, Maria
,
Tauber, Maithé
,
Jouret, Béatrice
,
Kieffer, Isabelle
,
Deltas, Constantinos
,
Tanteles, George A.
,
Anastasiadou, Violetta
,
Patsalis, Philippos C.
,
Sismani, Carolina
Published in
Gene
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The Cypriot and Iranian National Mutation Frequency Databases
by
Kleanthous, Marina
,
Patsalis, Philippos C.
,
Drousiotou, Anthi
,
Motazacker, Mehdi
,
Christodoulou, Kyproula
,
Cariolou, Marios
,
Baysal, Erol
,
Khrizi, Kimia
,
Moghimi, Babak
,
Pourfarzad, Farzin
,
van Baal, Sjozef
,
Deltas, Constantinos
,
Najmabadi, Hossein
,
Patrinos, George P.
Published in
Human mutation
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American Journal Of Medical Genetics. Part A
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Gene
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Human Mutation
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Genetic Testing
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Genetics & Heredity
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Humans
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Life Sciences & Biomedicine
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Science & Technology
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Adult
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Autosomal Recessive Inheritance
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Base Sequence
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Body Patterning - Genetics
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Cardiomyopathy
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Cardiomyopathy, Hypertrophic - Diagnosis
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Cardiomyopathy, Hypertrophic - Genetics
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Cardiomyopathy, Hypertrophic - Pathology
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Cell Line
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Connectin - Genetics
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Craniofacial
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Cypriot Population
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Cyprus - Epidemiology
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Databases, Genetic
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Developmental Defect
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