Minor facial anomalies in combined methylmalonic aciduria and homocystinuria due to a defect in cobalamin metabolism

被引：22

作者：

Cerone, R

Schiaffino, MC

Caruso, U

Lupino, S

Gatti, R

机构：

[1] Univ Genoa, Dept Pediat, G Gaslini Inst, I-16148 Genoa, Italy

[2] Univ Genoa, Div Pediat 3, I-16148 Genoa, Italy

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1999年 / 22卷 / 03期

关键词：

D O I：

10.1023/A:1005521702298

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：247 / 250

页数：4

共 6 条

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[3]

CERONE R, 1994, ARCH PEDIATRIE, V1, P762

[4]

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[5]

ROSENBLATT DS, 1986, PEDIATRICS, V78, P51

[6] Clinical heterogeneity and prognosis in combined methylmalonic aciduria and homocystinuria (cblC) [J].

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