[Detection rate and clinical significance of regions of homozygosity in prenatal genetic diagnosis].

Zhu, L F; Zhang, H M; Mai, L H; Sun, X F; Liu, W Q

Zhu, L F; Zhang, H M; Mai, L H; Sun, X F; Liu, W Q.

Affiliation

Zhu LF; Department of Obstetrics and Gynecology, Guangdong Provincal Key Laboratory of Major Obstetric Diseases, the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou 510150, China.
Zhang HM; Department of Obstetrics and Gynecology, Guangdong Provincal Key Laboratory of Major Obstetric Diseases, the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou 510150, China.
Mai LH; Department of Obstetrics and Gynecology, Guangdong Provincal Key Laboratory of Major Obstetric Diseases, the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou 510150, China.
Sun XF; Department of Obstetrics and Gynecology, Guangdong Provincal Key Laboratory of Major Obstetric Diseases, the Third Affiliated Hospital of Guangzhou Medical University, Guangzhou 510150, China.
Liu WQ; Central Laboratory, Shenzhen Longgang District Maternity and Child Healthcare Hospital, Shenzhen 518172, China.

Zhonghua Fu Chan Ke Za Zhi ; 57(4): 271-277, 2022 Apr 25.

Article in Zh | MEDLINE | ID: mdl-35484659

Subject(s)

Abnormal Karyotype; Prenatal Diagnosis; Female; Fetus; Humans; Pregnancy; Prenatal Care; Prenatal Diagnosis/methods; Retrospective Studies

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prenatal Diagnosis / Abnormal Karyotype Type of study: Diagnostic_studies / Observational_studies / Risk_factors_studies Limits: Female / Humans / Pregnancy Language: Zh Journal: Zhonghua Fu Chan Ke Za Zhi Year: 2022 Document type: Article Affiliation country: China Country of publication: China

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