BORJESON-FORSSMAN-LEHMANN SYNDROME - FURTHER DELINEATION IN 5 CASES

被引:22
作者
ARDINGER, HH [1 ]
HANSON, JW [1 ]
ZELLWEGER, HU [1 ]
机构
[1] UNIV IOWA,HOSP & CLIN,DEPT PEDIAT,DIV MED GENET,IOWA CITY,IA 52242
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1984年 / 19卷 / 04期
关键词
D O I
10.1002/ajmg.1320190405
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
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页码:653 / 664
页数:12
相关论文
共 7 条
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  • [2] BORJESON M, 1963, 2ND P INT C MENT R 1, P188
  • [3] BORJESON M, 1962, ACTA MED SCAND, V171, P12
  • [4] BRUN A, 1974, J MENT DEFIC RES, V18, P317
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    ROBINSON, LK
    JONES, KL
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    NYHAN, WL
    SAKATI, N
    JONES, KL
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 15 (03): : 457 - 468
  • [6] VEALL RM, 1979, J MENT DEFIC RES, V23, P231
  • [7] PRIMARY HYPOGONADISM IN BORJESON-FORSSMAN-LEHMANN SYNDROME
    WEBER, FT
    FRIAS, JL
    JULIUS, RL
    FELMAN, AH
    [J]. JOURNAL OF MEDICAL GENETICS, 1978, 15 (01) : 63 - 66