A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1

被引:38
作者
Ahmad, W
Brancolini, V
ul Haque, MF
Lam, H
ul Haque, S
Haider, M
Maimon, A
Aita, VM
Owen, J
Brown, D
Zegarelli, DJ
Ahmad, M
Ott, J
Christiano, AM
机构
[1] Rockefeller Univ, Dept Dermatol, New York, NY 10027 USA
[2] Rockefeller Univ, Dept Genet & Dev, New York, NY 10027 USA
[3] Rockefeller Univ, Sch Dent & Oral Surg, New York, NY 10027 USA
[4] Rockefeller Univ, Lab Stat Genet, New York, NY 10021 USA
[5] Quaid I Azam Univ, Dept Biol Sci, Islamabad, Pakistan
[6] Abbassi Shaheed Hosp, Karachi, Pakistan
[7] Res Genet Inc, Huntsville, AL 35801 USA
关键词
D O I
10.1086/301799
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:987 / 991
页数:5
相关论文
共 15 条
[11]   Two genes for missing teeth [J].
Thesleff, I .
NATURE GENETICS, 1996, 13 (04) :379-380
[12]   The enamel knot as a signaling center in the developing mouse tooth [J].
Vaahtokari, A ;
Aberg, T ;
Jernvall, J ;
Keranen, S ;
Thesleff, I .
MECHANISMS OF DEVELOPMENT, 1996, 54 (01) :39-43
[13]  
Vaahtokari A, 1996, DEVELOPMENT, V122, P121
[14]  
VAINIO S, 1993, CELL, V75, P45, DOI 10.1016/0092-8674(93)90678-J
[15]   A human MSX1 homeodomain missense mutation causes selective tooth agenesis [J].
Vastardis, H ;
Karimbux, N ;
Guthua, SW ;
Seidman, JG ;
Seidman, CE .
NATURE GENETICS, 1996, 13 (04) :417-421