Cristina Dragomir - Genetic Lab, Laboratory of Medical Genetics, Bucharest, Romania

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论文共 18 篇作者统计合作学者相似作者

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Impact of Prenatal Ultrasound Findings and Parental SNP Microarray Testing in Pregnancy Management

Irina Ioana Iordanescu, Anca Teodora Neacsu,Mariela Sanda Militaru,Andreea Catana, Zina Barabas Cuzmici, Diana Elena Voicu,Cristina Dragomir,Emilia Severin

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 105-105

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Microduplication and Microdeletion Syndromes Diagnosed Prenatally Using Single Nucleotide Polymorphism Array

Irina Ioana Iordanescu,Andreea Catana, Zina Barabas Cuzmici,Iuliana Chelu,Cristina Dragomir, Maria Militaru,Emilia Severin,Mariela Sanda Militaru

JOURNAL OF PERSONALIZED MEDICINEno. 3 (2024)

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Challenging Diagnoses of Tetraploidy/diploidy and Trisomy 12: Utility of First-Tier Prenatal Testing Methods

Irina Ioana Iordanescu, Anca Teodora Neacsu,Andreea Catana, Zina Barabas-CuzmicI, Viorel Suciu,Cristina Dragomir, Diana Elena Voicu,Emilia Severin,Mariela Sanda Militaru

Frontiers in genetics (2023)

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Genetic Variants and Biochemical Parameters Associated with the Risk for Venous Thromboembolism in a Romanian Cohort

Simona Topoleanu,Radu-Ioan Ursu,Laurentiu-Camil Bohiltea,Antoanela Curici,Natalia Cucu, Mihaela Popa, Andra Perioc,Andreea Ionescu, Patricia Riurean,Iuliana Chelu,Cristina Dragomir,Gratiela Chelu,Andreea Mirela Caragea, Radu Truica,Alexandra Cojocaru,Mariana Carmen Chifiriuc,Ileana Stoica

BIOINTERFACE RESEARCH IN APPLIED CHEMISTRYno. 4 (2022)

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Frequnecy of CFTR mutations in a Romanian cohort of individuals with cystic fibrosis

Georgiana Ilie,Viorica Radoi,Andreea Ionescu,Iuliana Chelu,Cristina Dragomir,Gratiela Chelu,Mihaela Popa,Bianca Basan-Giu, Andra Perioc,Oana Istrate, Traian Grozescu,Paul Iordache,Lucian Pop,Natalia Cucu,Camil Laurentiu Bohiltea,Radu-Ioan Ursu

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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Genetic testing algorithms for fetal malformations malformations

Viorica Radoi,Radu-Ioan Ursu,Cristina Dragomir,Andreea Ionescu,Iuliana Chelu,Laurentiu Camil Bohiltea

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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ArrayCGH for the diagnosis of a ring X Turner syndrome variant

Viorica Elena Radoi,Oana Istrate,Marinela Malageanu,Sandra Grigore,Gratiela Chelu,Cristina Dragomir,Bianca Basangiu,Roxana Bohiltea,Laurentiu-Camil Bohiltea,Radu-Ioan Ursu

MOLECULAR CYTOGENETICSno. SUPnan (2017)

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A case of a non mosaic trisomy 22 in a 7 months old girl

Radu-Ioan Ursu,Sandra Grigore,Marinela Malageanu,Oana Istrate,Gratiela Chelu,Cristina Dragomir,Bianca Basangiu,Roxana Bohiltea,Camil Laurentiu Bohiltea,Viorica Elena Radoi

MOLECULAR CYTOGENETICSno. SUPnan (2017)

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Oro-dental Phenotypes Associated with Rare Monogenic Disorders

Severin Emilia,Dinca Octavian,Vladan Cristian, Bodnar Dana,Cristina Dragomir,Bucur Alexandru

openalex（2016）

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The Noninvasive Fetal RHD Genotyping from Cell-Free Fetal DNA Circulating in Maternal Blood: A Feasible Tool in Clinical Practice of Mother-Fetus Rh Incompatibility in Romania

Ionescu Adriana Maria,Dragomir Cristina,Severin Emilia,Schipor Sorina, Mierloi Daniela,Attila Cristian Ratiu, Badila Madalina, Ionescu Mirela, Albu Dinu,Stefanescu Dragos,Savu Lorand

ROMANIAN BIOTECHNOLOGICAL LETTERS（2016）

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