学术探索
学术期刊
新闻热点
数据分析
智能评审

BORJESON-FORSSMAN-LEHMANN SYNDROME - CLINICAL MANIFESTATIONS AND GENE LOCALIZATION TO XQ26-27

被引：57
作者：
TURNER, G
GEDEON, A
MULLEY, J
SUTHERLAND, G
RAE, J
POWER, K
ARTHUR, I
机构：
[1] ADELAIDE CHILDRENS HOSP INC,DEPT HISTOPATHOL,ADELAIDE,SA 5006,AUSTRALIA
[2] PRINCE WALES CHILDRENS HOSP,DEPT MED GENET,SYDNEY,AUSTRALIA
[3] COMMUNITY HLTH CTR,TAMWORTH,NSW,AUSTRALIA
[4] COMMUNITY HLTH CTR,ARMIDALE,NSW,AUSTRALIA
[5] COMMUNITY HLTH CTR,SAWTELL,NSW,AUSTRALIA
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1989年 / 34卷 / 04期
关键词：
D O I：
10.1002/ajmg.1320340402
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：463 / 469
页数：7
相关论文
共 10 条
  • [1] BORJESON-FORSSMAN-LEHMANN SYNDROME - FURTHER DELINEATION IN 5 CASES
    ARDINGER, HH
    HANSON, JW
    ZELLWEGER, HU
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 19 (04): : 653 - 664
  • [2] BORJESON M, 1962, ACTA MED SCAND, V171, P12
  • [3] REPORT OF THE COMMITTEE ON THE GENETIC CONSTITUTION OF THE X-CHROMOSOMES AND Y-CHROMOSOMES
    DAVIES, KE
    MANDEL, JL
    WEISSENBACH, J
    FELLOUS, M
    [J]. CYTOGENETICS AND CELL GENETICS, 1987, 46 (1-4): : 277 - 315
  • [4] DEREYMAEKER AM, 1986, CLIN GENET, V29, P317
  • [5] PROBABLE LOCALIZATION OF THE COFFIN-LOWRY LOCUS IN XP22.2-P22.1 BY MULTIPOINT LINKAGE ANALYSIS
    HANAUER, A
    ALEMBIK, Y
    GILGENKRANTZ, S
    MUJICA, P
    NIVELONCHEVALLIER, A
    PEMBREY, ME
    YOUNG, ID
    MANDEL, JL
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (1-2): : 523 - 530
  • [6] LINKAGE AND GENETIC-COUNSELING FOR THE FRAGILE-X USING DNA PROBE-52A, PROBE-F9, PROBE-DX13, AND PROBE-ST14
    MULLEY, JC
    GEDEON, AK
    THORN, KA
    BATES, LJ
    SUTHERLAND, GR
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 27 (02): : 435 - 448
  • [7] A FAMILY WITH THE COFFIN LOWRY SYNDROME REVISITED - LOCALIZATION OF CLS TO XP21-PTER
    PARTINGTON, MW
    MULLEY, JC
    SUTHERLAND, GR
    THODE, A
    TURNER, G
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (1-2): : 509 - 521
  • [8] THE BORJESON-FORSSMAN-LEHMANN SYNDROME
    ROBINSON, LK
    JONES, KL
    CULLER, F
    NYHAN, WL
    SAKATI, N
    JONES, KL
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 15 (03): : 457 - 468
  • [9] X-LINKED HYPOGONADISM, GYNECOMASTIA, MENTAL-RETARDATION, SHORT STATURE, AND OBESITY - NEW SYNDROME
    VASQUEZ, SB
    HURST, DL
    SOTOS, JF
    [J]. JOURNAL OF PEDIATRICS, 1979, 94 (01) : 56 - 60
  • [10] REPORT OF THE COMMITTEE ON HUMAN-GENE MAPPING BY RECOMBINANT DNA TECHNIQUES
    WILLARD, HF
    SKOLNICK, MH
    PEARSON, PL
    MANDEL, JL
    [J]. CYTOGENETICS AND CELL GENETICS, 1985, 40 (1-4): : 360 - 489
1