[Early prenatal genetic diagnosis of oculocutaneous albinism type I in seven families].

Wu, Qinghua; Shi, Hui-rong; Liu, Ning; Lu, Ning; Jiang, Miao; Zhao, Zhen-hua; Kong, Xiang-dong

Wu, Qinghua; Shi, Hui-rong; Liu, Ning; Lu, Ning; Jiang, Miao; Zhao, Zhen-hua; Kong, Xiang-dong.

Affiliation

Wu Q; Center of Prenatal Diagnosis, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 29(4): 377-81, 2012 Aug.

Article in Zh | MEDLINE | ID: mdl-22875490

Subject(s)

Albinism, Oculocutaneous/diagnosis; Albinism, Oculocutaneous/genetics; Albinism, Oculocutaneous/enzymology; Female; Genetic Predisposition to Disease; Humans; Infant, Newborn; Male; Monophenol Monooxygenase/genetics; Mutation; Pedigree; Pregnancy; Prenatal Diagnosis/methods

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Albinism, Oculocutaneous Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male / Newborn / Pregnancy Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2012 Document type: Article Country of publication: China

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