Prenatal Sonographic Features of Rare Chromosome 13 Aberrations.

Moczulska, Hanna; Pietrusinski, Michal; Serafin, Marcin; Skoczylas, Beata; Sieroszewski, Piotr; Borowiec, Maciej

Moczulska, Hanna; Pietrusinski, Michal; Serafin, Marcin; Skoczylas, Beata; Sieroszewski, Piotr; Borowiec, Maciej.

Afiliação

Moczulska H; Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland.
Pietrusinski M; Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland.
Serafin M; Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland.
Skoczylas B; Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland.
Sieroszewski P; Department of Fetal Medicine and Gynecology, Medical University of Lodz, Lodz, Poland.
Borowiec M; Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland.

Appl Clin Genet ; 15: 145-151, 2022.

Article em En | MEDLINE | ID: mdl-36213554

Palavras-chave

amniocentesis; chromosome 13; karyotype; prenatal testing

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Appl Clin Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Polônia País de publicação: Nova Zelândia

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