THE PROPAGATION OF INSOLVENCY AMONG BUSINESS IN ROMANIA by Ioana Maria BUCERZAN

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Cluster Analysis on Cohesion Policy Towards Europe 2020 Strategy for Smart, Sustainable and Inclusive Growth by Ramona Camelia BERE, Ioana BUCERZAN (PRECUP)

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Aspects of a Watermark Solution by Dominic BUCERZAN, Crina RATIU, Ioan DASCAL

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16q24.3 Microduplication in a Patient With Developmental Delay, Intellectual Disability, Short Stature, and Nonspecific Dysmorphic Features: Case Report and Review of the Literatur... by Simona Bucerzan, Simona Bucerzan, Diana Miclea, Diana Miclea, Cecilia Lazea, Cecilia Lazea, Carmen Asavoaie, Andrea Kulcsar, Paula Grigorescu-Sido

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Characteristics of the Population of Romania During 1990–2013 by Tudorel ANDREI, Bogdan OANCEA, Claudia CĂPĂŢÂNĂ, Ioana BUCERZAN (PRECUP)

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46,XX DSD: Developmental, Clinical and Genetic Aspects by Camelia Alkhzouz, Simona Bucerzan, Maria Miclaus, Andreea-Manuela Mirea, Diana Miclea

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Is there a correlation between GAD2 gene-243 A>G polymorphism and obesity? by Alkhzouz Camelia, Miclea Diana, Farcas Marius, Bucerzan Simona, Cabau Georgiana, Popp Radu Anghel

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Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study) by Bucerzan S, Miclea D, Popp R, Alkhzouz C, Lazea C, Pop IV, Grigorescu-Sido P

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Evaluation of c677t and a1298c polymorphism of the methylenetetrahydrofolate reductase gene as a maternal risk factor for trisomy 21 (a monocentric study) by Bucerzan Simona, Popp Radu Anghel, Vlad Raluca Maria, Lazea Cecilia, Nicolaescu Radu, Grigorescu-Sido Paula

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SINDROMUL MALFORMATIV LA PACIENŢII CU TRISOMIE 21 by Raluca Maria Vlad, Paula Grigorescu Sido, Simona Bucerzan, Camelia Al-Khzouz, Ioana Naşcu, Eugen Pascal Ciofu

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Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1 by Zimmermann A, Popp RA, Rossmann H, Bucerzan S, Nascu I, Leucuta D, Weber MM, Grigorescu-Sido P

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MODIFICĂRI HEMATOLOGICE LA PACIENŢII CU TRISOMIE 21 by Raluca Maria Vlad, Paula Grigorescu Sido, Simona Bucerzan, Camelia Al-Khzouz, Ioana Naşcu, Eugen Pascal Ciofu

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Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis Patients by Alkhzouz C, Cabau G, Lazea C, Asavoaie C, Bucerzan S, Mirea AM, Farcas M, Miclaus M Jnr, Popp R, Miclea D

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Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability by Diana Miclea, Sergiu Osan, Simona Bucerzan, Delia Stefan, Radu Popp, Monica Mager, Maria Puiu, Cristian Zimbru, Adela Chirita-Emandi, Camelia Alkhzouz

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Molecular and Cytogenetic Analysis of Romanian Patients with Differences in Sex Development by Diana Miclea, Camelia Alkhzouz, Simona Bucerzan, Paula Grigorescu-Sido, Radu Anghel Popp, Ionela Maria Pascanu, Victoria Cret, Cristina Ghervan, Ligia Blaga, Gabriela Zaharie

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Cardiac Manifestations in a Group of Romanian Patients with Gaucher Disease Type 1 (a Monocentric Study) by Cecilia Lazea, Simona Bucerzan, Camelia Al-Khzouz, Anca Zimmermann, Ștefan Cristian Vesa, Ioana Nașcu, Victoria Creț, Mirela Crișan, Carmen Asăvoaie, Diana Miclea, Paula Grigorescu-Sido

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Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability by Miclea D, Szucs A, Mirea AM, Stefan DM, Nazarie F, Bucerzan S, Lazea C, Grama A, Pop TL, Farcas M, Zaharie G, Matyas M, Mager Snr M, Vintan M, Popp R, Alkhzouz C

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