Growing interest in Turner syndrome

被引:9
作者
Zinn, AR [1 ]
机构
[1] UNIV TEXAS,SW MED SCH,DEPT INTERNAL MED,DALLAS,TX 75235
关键词
D O I
10.1038/ng0597-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
[No abstract available]
引用
收藏
页码:3 / 4
页数:2
相关论文
共 12 条
[1]  
FERGUSON-SMITH M A, 1965, J Med Genet, V2, P142, DOI 10.1136/jmg.2.2.142
[2]   HOMOLOGOUS RIBOSOMAL-PROTEIN GENES ON THE HUMAN X-CHROMOSOME AND Y-CHROMOSOME - ESCAPE FROM X-INACTIVATION AND POSSIBLE IMPLICATIONS FOR TURNER SYNDROME [J].
FISHER, EMC ;
BEERROMERO, P ;
BROWN, LG ;
RIDLEY, A ;
MCNEIL, JA ;
LAWRENCE, JB ;
WILLARD, HF ;
BIEBER, FR ;
PAGE, DC .
CELL, 1990, 63 (06) :1205-1218
[3]  
FORD CE, 1959, LANCET, V1, P711
[4]   CAMPOMELIC DYSPLASIA AND AUTOSOMAL SEX REVERSAL CAUSED BY MUTATIONS IN AN SRY-RELATED GENE [J].
FOSTER, JW ;
DOMINGUEZSTEGLICH, MA ;
GUIOLI, S ;
KWOK, C ;
WELLER, PA ;
STEVANOVIC, M ;
WEISSENBACH, J ;
MANSOUR, S ;
YOUNG, ID ;
GOODFELLOW, PN ;
BROOK, JD ;
SCHAFER, AJ .
NATURE, 1994, 372 (6506) :525-530
[5]  
LYON MF, 1962, AM J HUM GENET, V14, P135
[6]   The molecular basis of hypodactyly (Hd): A deletion in Hoxa13 leads to arrest of digital arch formation [J].
Mortlock, DP ;
Post, LC ;
Innis, JW .
NATURE GENETICS, 1996, 13 (03) :284-289
[7]  
OGATA T, 1992, J MED GENET, V29, P455
[8]   RUBINSTEIN-TAYBI SYNDROME CAUSED BY MUTATIONS IN THE TRANSCRIPTIONAL COACTIVATOR CBP [J].
PETRIJ, F ;
GILES, RH ;
DAUWERSE, HG ;
SARIS, JJ ;
HENNEKAM, RCM ;
MASUNO, M ;
TOMMERUP, N ;
VANOMMEN, GJB ;
GOODMAN, RH ;
PETERS, DJM ;
BREUNING, MH .
NATURE, 1995, 376 (6538) :348-351
[9]   Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome [J].
Rao, E ;
Weiss, B ;
Fukami, M ;
Rump, A ;
Niesler, B ;
Mertz, A ;
Muroya, K ;
Binder, G ;
Kirsch, S ;
Winkelmann, M ;
Nordsiek, G ;
Heinrich, U ;
Breuning, MH ;
Ranke, MB ;
Rosenthal, A ;
Ogata, T ;
Rappold, GA .
NATURE GENETICS, 1997, 16 (01) :54-63
[10]  
ROSS JL, IN PRESS AM J MED GE