FG SYNDROME - FURTHER CHARACTERIZATION, REPORT OF A 3RD FAMILY, AND OF A SPORADIC CASE

被引:28
作者
RICCARDI, VM
HASSLER, E
LUBINSKY, MS
机构
[1] BAYLOR UNIV,COLL MED,TEXAS MED CTR,KLEBERG CTR HUMAN GENET,HOUSTON,TX 77030
[2] FRIEDRICH SCHILLER UNIV,DEPT PEDIAT,DDR-69 JENA,GER DEM REP
[3] UNIV WISCONSIN,CTR HLTH SCI & MED SCH,DEPT PEDIAT,MADISON,WI 53706
[4] UNIV WISCONSIN,CTR HLTH SCI & MED SCH,DEPT MED GENET,WISCONSIN CLIN GENET CTR,MADISON,WI 53706
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1977年 / 1卷 / 01期
关键词
D O I
10.1002/ajmg.1320010106
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:47 / 58
页数:12
相关论文
共 9 条
  • [1] CHILDS B, 1976, AM J HUM GENET, V18, P537
  • [2] NEW SYNDROME OF MENTAL DEFICIENCY WITH CRANIOFACIAL, LIMB, AND ANAL ABNORMALITIES
    KELLER, MA
    JONES, KL
    NYHAN, WL
    FRANCKE, U
    DIXSON, B
    [J]. JOURNAL OF PEDIATRICS, 1976, 88 (04) : 589 - 591
  • [3] KELLER MA, 1976, J PEDIATR-US, V89, P687, DOI 10.1016/S0022-3476(76)80431-3
  • [4] STUDIES OF MALFORMATION SYNDROMES OF MAN XXXIII - FG SYNDROME - X-LINKED RECESSIVE SYNDROME OF MULTIPLE CONGENITAL ANOMALIES AND MENTAL-RETARDATION
    OPITZ, JM
    KAVEGGIA, EG
    [J]. ZEITSCHRIFT FUR KINDERHEILKUNDE, 1974, 117 (01): : 1 - 18
  • [5] OPITZ JM, 1976, J PEDIATR-US, V89, P687, DOI 10.1016/S0022-3476(76)80429-5
  • [6] Riccardi V. M., 1977, GENETIC APPROACH HUM
  • [7] RICCARDI VM, 1977, GENETIC APPROACH HUM, P261
  • [8] RICCARDI VM, 1976, AM J PUBL HLTH, V86, P268
  • [9] RICCARDI VM, IN PRESS