THE OPITZ SYNDROME - A NEW DESIGNATION FOR THE CLINICALLY INDISTINGUISHABLE BBB-SYNDROME AND G-SYNDROME

被引:40
作者
CAPPA, M
BORRELLI, P
MARINI, R
NERI, G
机构
[1] UNIV CATTOLICA SACRO CUORE, FAC MED A GEMELLI, IST GENET UMANA, LARGO F VITO 1, I-00168 ROME, ITALY
[2] UNIV CATTOLICA SACRO CUORE, OSPED BAMBINO GESU, IST RICERCA SCI, REPARTO ENDOCRINOL PEDIAT, I-00168 ROME, ITALY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 28卷 / 02期
关键词
D O I
10.1002/ajmg.1320280207
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:303 / 309
页数:7
相关论文
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[2]   G AND BBB SYNDROMES - CASE PRESENTATIONS, GENETICS, AND NOSOLOGY [J].
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[3]  
Opitz, 1969, BIRTH DEFECTS OAS, VV, P95
[4]  
Opitz J. M., 1969, BIRTH DEFECTS AOS, VV, P86
[5]   G-SYNDROME (HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS, OR HYPOSPADIAS-DYSPHAGIA, OR OPITZ-FRIAS OR OPITZ-G SYNDROME) - PERSPECTIVE IN 1987 AND BIBLIOGRAPHY [J].
OPITZ, JM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (02) :275-285
[6]  
Smith, 1982, RECOGNIZABLE PATTERN