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

被引：37
|
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
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1998年 / 62卷 / 04期
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 50 条
  • [21] Mapping of an autosomal recessive congenital cataract locus to chromosome 9q.
    Forshew, T
    Johnson, CA
    Willis, C
    Moore, AT
    Maher, ER
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 489 - 489
  • [22] A first locus for isolated autosomal recessive optic atrophy (ROA1) maps to chromosome 8q
    Fabienne Barbet
    Sylvie Gerber
    Sélim Hakiki
    Isabelle Perrault
    Sylvain Hanein
    Dominique Ducroq
    Gaëlle Tanguy
    Jean-Louis Dufier
    Arnold Munnich
    Jean-Michel Rozet
    Josseline Kaplan
    European Journal of Human Genetics, 2003, 11 : 966 - 971
  • [23] A first locus for isolated autosomal recessive optic atrophy (ROA1) maps to chromosome 8q.
    Barbet, F
    Gerber, S
    Dufier, JL
    Munnich, A
    Rozet, J
    Kaplan, J
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2004, 45 : U513 - U513
  • [24] A first locus for isolated autosomal recessive optic atrophy (ROA1) maps to chromosome 8q
    Barbet, F
    Gerber, S
    Hakiki, S
    Perrault, I
    Hanein, S
    Ducroq, D
    Tanguy, G
    Dufier, JL
    Munnich, A
    Rozet, JM
    Kaplan, J
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2003, 11 (12) : 966 - 971
  • [25] A locus for autosomal recessive pseudoxanthoma elasticum, with penetrance of vascular symptoms in carriers, maps to chromosome 16p13.1
    vanSoest, S
    Swart, J
    Tijmes, N
    Sandkuijl, LA
    Rommers, J
    Bergen, AAB
    GENOME RESEARCH, 1997, 7 (08): : 830 - 834
  • [26] A first locus for isolated autosomal recessive optic atrophy (ROA1) maps to chromosome 8q
    Barbet, F
    Gerber, S
    Hakiki, S
    Perrault, I
    Hanein, S
    Ducroq, D
    Tanguy, G
    Dufier, JL
    Munnich, A
    Rozet, JM
    Kaplan, J
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 506 - 506
  • [27] A PARACENTRIC INVERSION OF 16Q IN A PATIENT WITH ANUS, HAND, AND EAR ANOMALIES - FURTHER EVIDENCE FOR A TOWNES-BROCKS SYNDROME GENE AT 16Q12.1
    POWELL, CM
    REITNAUER, PJ
    KAISERROGERS, KA
    RAO, KW
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 552 - 552
  • [28] Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9
    Ikeuchi, T
    Asaka, T
    Saito, M
    Tanaka, H
    Higuchi, S
    Tanaka, K
    Saida, K
    Uyama, E
    Mizusawa, H
    Fukuhara, N
    Nonaka, I
    Takamori, M
    Tsuji, S
    ANNALS OF NEUROLOGY, 1997, 41 (04) : 432 - 437
  • [29] A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23
    Dick, K. J.
    Al-Mjeni, R.
    Baskir, W.
    Koul, R.
    Simpson, M. A.
    Patton, M. A.
    Raeburn, S.
    Crosby, A. H.
    NEUROLOGY, 2008, 71 (04) : 248 - 252
  • [30] A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22
    Campbell, DA
    McHale, DP
    Brown, KA
    Moynihan, LM
    Houseman, M
    Karbani, G
    Parry, G
    Janjua, AH
    Newton, V
    Al-Gazali, L
    Markham, AF
    Lench, NJ
    Mueller, RF
    JOURNAL OF MEDICAL GENETICS, 1997, 34 (12) : 1015 - 1017
12345