Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities.

Najafi, Kimia; Mehrjoo, Zohreh; Ardalani, Fariba; Ghaderi-Sohi, Siavash; Kariminejad, Ariana; Kariminejad, Roxana; Najmabadi, Hossein

Najafi, Kimia; Mehrjoo, Zohreh; Ardalani, Fariba; Ghaderi-Sohi, Siavash; Kariminejad, Ariana; Kariminejad, Roxana; Najmabadi, Hossein.

Afiliação

Najafi K; Genetic Research Center, National Reference Laboratory for Prenatal Diagnosis, University of Social Welfare and Rehabilitation Sciences, Koodakyar Avenue, Daneshjoo Blvd, Evin, Tehran, 1985713834, Iran.
Mehrjoo Z; Kariminejad-Najmabadi Pathology and Genetics Center, #2, West Side of Sanat Sq.-Metro Station, Shahrak Gharb, Tehran, 1466713713, Iran.
Ardalani F; Genetic Research Center, National Reference Laboratory for Prenatal Diagnosis, University of Social Welfare and Rehabilitation Sciences, Koodakyar Avenue, Daneshjoo Blvd, Evin, Tehran, 1985713834, Iran.
Ghaderi-Sohi S; Genetic Research Center, National Reference Laboratory for Prenatal Diagnosis, University of Social Welfare and Rehabilitation Sciences, Koodakyar Avenue, Daneshjoo Blvd, Evin, Tehran, 1985713834, Iran.
Kariminejad A; Kariminejad-Najmabadi Pathology and Genetics Center, #2, West Side of Sanat Sq.-Metro Station, Shahrak Gharb, Tehran, 1466713713, Iran.
Kariminejad R; Kariminejad-Najmabadi Pathology and Genetics Center, #2, West Side of Sanat Sq.-Metro Station, Shahrak Gharb, Tehran, 1466713713, Iran.
Najmabadi H; Kariminejad-Najmabadi Pathology and Genetics Center, #2, West Side of Sanat Sq.-Metro Station, Shahrak Gharb, Tehran, 1466713713, Iran.

Sci Rep ; 11(1): 6952, 2021 03 26.

Article em En | MEDLINE | ID: mdl-33772059

Assuntos

Aborto Habitual/genética; Consanguinidade; Sequenciamento do Exoma/métodos; Aberrações Cromossômicas; Variações do Número de Cópias de DNA/genética; Feminino; Testes Genéticos; Idade Gestacional; Humanos; Irã (Geográfico); Masculino; Mutação/genética; Gravidez

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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Aborto Habitual / Consanguinidade / Sequenciamento do Exoma Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies Limite: Female / Humans / Male / Pregnancy País/Região como assunto: Asia Idioma: En Revista: Sci Rep Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Irã

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