学术探索
学术期刊
新闻热点
数据分析
智能评审
立即登录
Localization of a gene for nonspecific X-linked mental retardation (MRX 76) to Xp22.3-Xp21.3
被引:5
作者
:
Kleefstra, T
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen, Dept Human Genet, Med Ctr St Radboud, Nijmegen, Netherlands
Kleefstra, T
Yntema, HG
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen, Dept Human Genet, Med Ctr St Radboud, Nijmegen, Netherlands
Yntema, HG
Oudakker, AR
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen, Dept Human Genet, Med Ctr St Radboud, Nijmegen, Netherlands
Oudakker, AR
de Vries, BBA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen, Dept Human Genet, Med Ctr St Radboud, Nijmegen, Netherlands
de Vries, BBA
van Bokhoven, H
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen, Dept Human Genet, Med Ctr St Radboud, Nijmegen, Netherlands
van Bokhoven, H
Hamel, BCJ
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen, Dept Human Genet, Med Ctr St Radboud, Nijmegen, Netherlands
Hamel, BCJ
Poppelaars, FA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen, Dept Human Genet, Med Ctr St Radboud, Nijmegen, Netherlands
Poppelaars, FA
Ausems, MGEM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen, Dept Human Genet, Med Ctr St Radboud, Nijmegen, Netherlands
Ausems, MGEM
机构
:
[1]
Univ Nijmegen, Dept Human Genet, Med Ctr St Radboud, Nijmegen, Netherlands
[2]
Free Univ Amsterdam, Dept Human Genet, Ctr Med, Amsterdam, Netherlands
[3]
Univ Utrecht, Ctr Med, Dept Med Genet, Utrecht, Netherlands
来源
:
AMERICAN JOURNAL OF MEDICAL GENETICS
|
2002年
/ 110卷
/ 04期
关键词
:
D O I
:
10.1002/ajmg.10483
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
引用
收藏
页码:410 / 411
页数:2
相关论文
共 4 条
[1]
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation
Bienvenu, T
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Bienvenu, T
Poirier, K
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Poirier, K
Friocourt, G
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Friocourt, G
Bahi, N
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Bahi, N
Beaumont, D
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Beaumont, D
Fauchereau, F
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Fauchereau, F
Ben Jeema, L
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Ben Jeema, L
Zemni, R
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Zemni, R
Vinet, MC
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Vinet, MC
Francis, F
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Francis, F
Couvert, P
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Couvert, P
Gomot, M
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Gomot, M
Moraine, C
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Moraine, C
van Bokhoven, H
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
van Bokhoven, H
Kalscheuer, V
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Kalscheuer, V
Frints, S
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Frints, S
Gecz, J
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Gecz, J
Ohzaki, K
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Ohzaki, K
Chaabouni, H
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Chaabouni, H
Fryns, JP
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Fryns, JP
Desportes, V
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Desportes, V
Beldjord, C
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Beldjord, C
Chelly, J
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Chelly, J
[J].
HUMAN MOLECULAR GENETICS,
2002,
11
(08)
: 981
-
991
[2]
A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation
Carrié, A
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Carrié, A
Jun, L
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Jun, L
Bienvenu, T
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Bienvenu, T
Vinet, MC
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Vinet, MC
McDonell, N
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
McDonell, N
Couvert, P
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Couvert, P
Zemni, R
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Zemni, R
Cardona, A
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Cardona, A
Van Buggenhout, G
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Van Buggenhout, G
Frints, S
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Frints, S
Hamel, B
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Hamel, B
Moraine, C
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Moraine, C
Ropers, HH
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Ropers, HH
Strom, T
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Strom, T
Howell, GR
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Howell, GR
Whittaker, A
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Whittaker, A
Ross, MT
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Ross, MT
Kahn, A
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Kahn, A
Fryns, JP
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Fryns, JP
Beldjord, C
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Beldjord, C
Marynen, P
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Marynen, P
Chelly, J
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Chelly, J
[J].
NATURE GENETICS,
1999,
23
(01)
: 25
-
31
[3]
XLMR genes: update 2000
Chiurazzi, P
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Cattolica Sacro Cuore, Ist Genet Med, I-00168 Rome, Italy
Chiurazzi, P
Hamel, BCJ
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Cattolica Sacro Cuore, Ist Genet Med, I-00168 Rome, Italy
Hamel, BCJ
论文数:
引用数:
h-index:
机构:
Neri, G
[J].
EUROPEAN JOURNAL OF HUMAN GENETICS,
2001,
9
(02)
: 71
-
81
[4]
ETIOLOGICAL SURVEY OF SEVERELY RETARDED HERTFORDSHIRE CHILDREN WHO WERE BORN BETWEEN JANUARY 1, 1965 AND DECEMBER 31, 1967
LAXOVA, R
论文数:
0
引用数:
0
h-index:
0
机构:
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
LAXOVA, R
RIDLER, MAC
论文数:
0
引用数:
0
h-index:
0
机构:
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
RIDLER, MAC
BOWENBRAVERY, M
论文数:
0
引用数:
0
h-index:
0
机构:
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
BOWENBRAVERY, M
[J].
AMERICAN JOURNAL OF MEDICAL GENETICS,
1977,
1
(01):
: 75
-
86
←
1
→
共 4 条
[1]
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation
Bienvenu, T
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Bienvenu, T
Poirier, K
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Poirier, K
Friocourt, G
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Friocourt, G
Bahi, N
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Bahi, N
Beaumont, D
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Beaumont, D
Fauchereau, F
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Fauchereau, F
Ben Jeema, L
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Ben Jeema, L
Zemni, R
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Zemni, R
Vinet, MC
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Vinet, MC
Francis, F
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Francis, F
Couvert, P
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Couvert, P
Gomot, M
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Gomot, M
Moraine, C
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Moraine, C
van Bokhoven, H
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
van Bokhoven, H
Kalscheuer, V
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Kalscheuer, V
Frints, S
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Frints, S
Gecz, J
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Gecz, J
Ohzaki, K
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Ohzaki, K
Chaabouni, H
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Chaabouni, H
Fryns, JP
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Fryns, JP
Desportes, V
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Desportes, V
Beldjord, C
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Beldjord, C
Chelly, J
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin Port Royal, Inst Cochin, Lab Genet & Physiopathol Retards Mentaux, F-75014 Paris, France
Chelly, J
[J].
HUMAN MOLECULAR GENETICS,
2002,
11
(08)
: 981
-
991
[2]
A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation
Carrié, A
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Carrié, A
Jun, L
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Jun, L
Bienvenu, T
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Bienvenu, T
Vinet, MC
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Vinet, MC
McDonell, N
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
McDonell, N
Couvert, P
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Couvert, P
Zemni, R
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Zemni, R
Cardona, A
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Cardona, A
Van Buggenhout, G
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Van Buggenhout, G
Frints, S
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Frints, S
Hamel, B
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Hamel, B
Moraine, C
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Moraine, C
Ropers, HH
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Ropers, HH
Strom, T
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Strom, T
Howell, GR
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Howell, GR
Whittaker, A
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Whittaker, A
Ross, MT
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Ross, MT
Kahn, A
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Kahn, A
Fryns, JP
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Fryns, JP
Beldjord, C
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Beldjord, C
Marynen, P
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Marynen, P
Chelly, J
论文数:
0
引用数:
0
h-index:
0
机构:
CHU Cochin, INSERM, U129, IGGM, F-75014 Paris, France
Chelly, J
[J].
NATURE GENETICS,
1999,
23
(01)
: 25
-
31
[3]
XLMR genes: update 2000
Chiurazzi, P
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Cattolica Sacro Cuore, Ist Genet Med, I-00168 Rome, Italy
Chiurazzi, P
Hamel, BCJ
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Cattolica Sacro Cuore, Ist Genet Med, I-00168 Rome, Italy
Hamel, BCJ
论文数:
引用数:
h-index:
机构:
Neri, G
[J].
EUROPEAN JOURNAL OF HUMAN GENETICS,
2001,
9
(02)
: 71
-
81
[4]
ETIOLOGICAL SURVEY OF SEVERELY RETARDED HERTFORDSHIRE CHILDREN WHO WERE BORN BETWEEN JANUARY 1, 1965 AND DECEMBER 31, 1967
LAXOVA, R
论文数:
0
引用数:
0
h-index:
0
机构:
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
LAXOVA, R
RIDLER, MAC
论文数:
0
引用数:
0
h-index:
0
机构:
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
RIDLER, MAC
BOWENBRAVERY, M
论文数:
0
引用数:
0
h-index:
0
机构:
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
HARPERBURY HOSP, KENNEDY GALTON CTR, RADLETT, HERTFORDSHIRE, ENGLAND
BOWENBRAVERY, M
[J].
AMERICAN JOURNAL OF MEDICAL GENETICS,
1977,
1
(01):
: 75
-
86
←
1
→