Search Results - Bucerzan S

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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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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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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