学术探索
学术期刊
新闻热点
数据分析
智能评审

INTERNATIONAL NOSOLOGY OF HERITABLE DISORDERS OF CONNECTIVE-TISSUE, BERLIN, 1986

被引：522
作者：
BEIGHTON, P
DEPAEPE, A
DANKS, D
FINIDORI, G
GEDDEDAHL, T
GOODMAN, R
HALL, JG
HOLLISTER, DW
HORTON, W
MCKUSICK, VA
OPITZ, JM
POPE, FM
PYERITZ, RE
RIMOIN, DL
SILLENCE, D
SPRANGER, JW
THOMPSON, E
TSIPOURAS, P
VILJOEN, D
WINSHIP, I
YOUNG, I
机构：
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 29卷 / 03期
关键词：
D O I：
10.1002/ajmg.1320290316
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：581 / 594
页数：14
相关论文
共 101 条
  • [1] 2 FORMS OF CUTIS LAXA PRESENTING IN NEWBORN PERIOD
    AGHA, A
    SAKATI, NO
    HIGGINBOTTOM, MC
    JONES, KL
    BAY, C
    NYHAN, WL
    [J]. ACTA PAEDIATRICA SCANDINAVICA, 1978, 67 (06): : 775 - 780
  • [2] EPIDERMOLYSIS BULLOSA DYSTROPHICA DOMINANS (PASINI) - PRIMARY STRUCTURAL DEFECT OF ANCHORING FIBRILS
    ANTONLAMPRECHT, I
    HASHIMOTO, I
    [J]. HUMAN GENETICS, 1976, 32 (01) : 69 - 76
  • [3] A NEW FORM OF EHLERS-DANLOS SYNDROME - FIBRONECTIN CORRECTS DEFECTIVE PLATELET-FUNCTION
    ARNESON, MA
    HAMMERSCHMIDT, DE
    FURCHT, LT
    KING, RA
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1980, 244 (02): : 144 - 147
  • [4] A RARE TUMOR - SUBUNGUAL CHONDROMA - REPORT OF A CASE
    AYALA, F
    LEMBO, G
    MONTESANO, M
    [J]. DERMATOLOGICA, 1983, 167 (06): : 339 - 340
  • [5] RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA - EVIDENCE FOR INCREASED COLLAGENASE AS A GENETIC CHARACTERISTIC IN CELL-CULTURE
    BAUER, EA
    EISEN, AZ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1978, 148 (05) : 1378 - 1387
  • [6] VARIANTS OF EHLERS-DANLOS SYNDROME - CLINICAL BIOCHEMICAL HAEMATOLOGICAL AND CHROMOSOMAL FEATURES OF 100 PATIENTS
    BEIGHTON, P
    PRICE, A
    LORD, J
    DICKSON, E
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 1969, 28 (03) : 228 - +
  • [7] DOMINANT AND RECESSIVE FORMS CUTIS LAXA
    BEIGHTON, P
    [J]. JOURNAL OF MEDICAL GENETICS, 1972, 9 (02) : 216 - &
  • [8] BEIGHTON P, 1983, S AFR MED J, V64, P772
  • [9] BEIGHTON P, 1984, CLIN GENET, V26, P308
  • [10] BEIGHTON P, 1985, CLIN GENET, V27, P472
12345678910