Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance.

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作者： Małgorzata J M,Nowaczyk ^[1] ; Melissa T,Carter ; Jie,Xu ; Marlene,Huggins ; Gordana,Raca ; Soma,Das ; Christa Lese,Martin ; Stuart,Schwartz ; Robert,Rosenfield ; Darrel J,Waggoner

作者单位： Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada. ^[1]

主题词儿童(Child);儿童, 学龄前(Child, Preschool);染色体缺失(Chromosome Deletion);染色体障碍(Chromosome Disorders);染色体, 人, 6对(Chromosomes, Human, Pair 6);细胞遗传学分析(Cytogenetic Analysis);发育障碍(Developmental Disabilities);面容(Facies);父亲(Fathers);女(雌)性(Female);胎儿生长迟缓(Fetal Growth Retardation);人类(Humans);婴儿(Infant);男(雄)性(Male);综合征(Syndrome)

DOI 10.1002/ajmg.a.32144

PMID 18203180

发布时间 2020-09-30

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American journal of medical genetics. Part A

2008年146A卷3期

354-60页

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Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance.

American journal of medical genetics. Part A

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American journal of medical genetics. Part A

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Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance.

American journal of medical genetics. Part A

相似文献

American journal of medical genetics. Part A

相关期刊

检索历史清除