学术探索
学术期刊
新闻热点
数据分析
智能评审
立即登录
Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3q22
被引:16
作者
:
Dollfus, H
论文数:
0
引用数:
0
h-index:
0
机构:
Fac Med Strasbourg, CNRS, INSERM, U184,LGME, F-67085 Strasbourg, France
Dollfus, H
Kumaramanickavel, G
论文数:
0
引用数:
0
h-index:
0
机构:
Fac Med Strasbourg, CNRS, INSERM, U184,LGME, F-67085 Strasbourg, France
Kumaramanickavel, G
Biswas, P
论文数:
0
引用数:
0
h-index:
0
机构:
Fac Med Strasbourg, CNRS, INSERM, U184,LGME, F-67085 Strasbourg, France
Biswas, P
Stoetzel, C
论文数:
0
引用数:
0
h-index:
0
机构:
Fac Med Strasbourg, CNRS, INSERM, U184,LGME, F-67085 Strasbourg, France
Stoetzel, C
Quillet, R
论文数:
0
引用数:
0
h-index:
0
机构:
Fac Med Strasbourg, CNRS, INSERM, U184,LGME, F-67085 Strasbourg, France
Quillet, R
Denton, M
论文数:
0
引用数:
0
h-index:
0
机构:
Fac Med Strasbourg, CNRS, INSERM, U184,LGME, F-67085 Strasbourg, France
Denton, M
Maw, M
论文数:
0
引用数:
0
h-index:
0
机构:
Fac Med Strasbourg, CNRS, INSERM, U184,LGME, F-67085 Strasbourg, France
Maw, M
Perrin-Schmitt, F
论文数:
0
引用数:
0
h-index:
0
机构:
Fac Med Strasbourg, CNRS, INSERM, U184,LGME, F-67085 Strasbourg, France
Perrin-Schmitt, F
机构
:
[1]
Fac Med Strasbourg, CNRS, INSERM, U184,LGME, F-67085 Strasbourg, France
[2]
Sankara Nethralaya Med Res Fdn, Chennai, India
[3]
Anandalok, Kolkata, W Bengal, India
[4]
Univ Otago, Dept Biochem, Dunedin, New Zealand
来源
:
JOURNAL OF MEDICAL GENETICS
|
2001年
/ 38卷
/ 07期
关键词
:
D O I
:
10.1136/jmg.38.7.470
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
引用
收藏
页码:470 / 471
页数:2
相关论文
共 22 条
[11]
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome
[J].
Howard, TD
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Howard, TD
;
Paznekas, WA
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Paznekas, WA
;
Green, ED
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Green, ED
;
Chiang, LC
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Chiang, LC
;
Ma, N
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Ma, N
;
DeLuna, RIO
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
DeLuna, RIO
;
Delgado, CG
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Delgado, CG
;
GonzalezRamos, M
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
GonzalezRamos, M
;
Kline, AD
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Kline, AD
;
Jabs, EW
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Jabs, EW
.
NATURE GENETICS,
1997,
15
(01)
:36
-41
[12]
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1
[J].
Johnson, D
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Johnson, D
;
Horsley, SW
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Horsley, SW
;
Moloney, DM
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Moloney, DM
;
Oldridge, M
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Oldridge, M
;
Twigg, SRF
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Twigg, SRF
;
Walsh, S
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Walsh, S
;
Barrow, M
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Barrow, M
;
Njolstad, PR
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Njolstad, PR
;
Kunz, J
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Kunz, J
;
Ashworth, GJ
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Ashworth, GJ
;
Wall, SA
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Wall, SA
;
Kearney, L
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Kearney, L
;
Wilkie, AOM
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Wilkie, AOM
.
AMERICAN JOURNAL OF HUMAN GENETICS,
1998,
63
(05)
:1282
-1293
[13]
DEFINITION OF THE BLEPHAROPHIMOSIS, PTOSIS, EPICANTHUS INVERSUS SYNDROME CRITICAL REGION AT CHROMOSOME 3Q23 BASED ON THE ANALYSIS OF CHROMOSOMAL-ANOMALIES
[J].
LAWSON, CT
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
LAWSON, CT
;
TOOMES, C
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
TOOMES, C
;
FRYER, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
FRYER, A
;
CARETTE, MJM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
CARETTE, MJM
;
TAYLOR, GM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
TAYLOR, GM
;
FUKUSHIMA, Y
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
FUKUSHIMA, Y
;
DIXON, MJ
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
DIXON, MJ
.
HUMAN MOLECULAR GENETICS,
1995,
4
(05)
:963
-967
[14]
Linkage of blepharophimosis syndrome in a large Indian pedigree to chromosome 7p
[J].
Maw, M
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Maw, M
;
Kar, B
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Kar, B
;
Biswas, J
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Biswas, J
;
Biswas, P
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Biswas, P
;
Nancarrow, D
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Nancarrow, D
;
Bridges, R
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Bridges, R
;
Kumaramanickavel, G
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Kumaramanickavel, G
;
Denton, M
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Denton, M
;
Badrinath, SS
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Badrinath, SS
.
HUMAN MOLECULAR GENETICS,
1996,
5
(12)
:2049
-2054
[15]
Pantke O A, 1975, Birth Defects Orig Artic Ser, V11, P190
[16]
SAETHRE-CHOTZEN SYNDROME
[J].
REARDON, W
论文数:
0
引用数:
0
h-index:
0
REARDON, W
;
WINTER, RM
论文数:
0
引用数:
0
h-index:
0
WINTER, RM
.
JOURNAL OF MEDICAL GENETICS,
1994,
31
(05)
:393
-396
[17]
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases
[J].
Rose, CSP
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Rose, CSP
;
Patel, P
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Patel, P
;
Reardon, W
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Reardon, W
;
Malcolm, S
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Malcolm, S
;
Winter, RM
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Winter, RM
.
HUMAN MOLECULAR GENETICS,
1997,
6
(08)
:1369
-1373
[18]
BLEPHAROPHIMOSIS SYNDROME IS LINKED TO CHROMOSOME 3Q
[J].
SMALL, KW
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
SMALL, KW
;
STALVEY, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
STALVEY, M
;
FISHER, L
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
FISHER, L
;
MULLEN, L
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
MULLEN, L
;
DICKEL, C
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
DICKEL, C
;
BEADLES, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
BEADLES, K
;
REIMER, R
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
REIMER, R
;
LESSNER, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
LESSNER, A
;
LEWIS, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
LEWIS, K
;
PERICAKVANCE, MA
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
PERICAKVANCE, MA
.
HUMAN MOLECULAR GENETICS,
1995,
4
(03)
:443
-448
[19]
BLEPHAROPHIMOSIS, PTOSIS, EPICANTHUS INVERSUS, AND PRIMARY AMENORRHEA - DOMINANT TRAIT
[J].
TOWNES, PL
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ROCHESTER,MED CTR,DEPT OBSTET & GYNECOL,ROCHESTER,NY 14627
UNIV ROCHESTER,MED CTR,DEPT OBSTET & GYNECOL,ROCHESTER,NY 14627
TOWNES, PL
;
MUECHLER, EK
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ROCHESTER,MED CTR,DEPT OBSTET & GYNECOL,ROCHESTER,NY 14627
UNIV ROCHESTER,MED CTR,DEPT OBSTET & GYNECOL,ROCHESTER,NY 14627
MUECHLER, EK
.
ARCHIVES OF OPHTHALMOLOGY,
1979,
97
(09)
:1664
-1666
[20]
MILD PHENOTYPIC MANIFESTATION OF A 7P15.3P21.2 DELETION
[J].
WANG, C
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MICHIGAN HOSP,DEPT PEDIAT & COMMUNICABLE DIS,D1109 MPB BOX 0718,ANN ARBOR,MI 48109
WANG, C
;
MAYNARD, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MICHIGAN HOSP,DEPT PEDIAT & COMMUNICABLE DIS,D1109 MPB BOX 0718,ANN ARBOR,MI 48109
MAYNARD, S
;
GLOVER, TW
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MICHIGAN HOSP,DEPT PEDIAT & COMMUNICABLE DIS,D1109 MPB BOX 0718,ANN ARBOR,MI 48109
GLOVER, TW
;
BIESECKER, LG
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MICHIGAN HOSP,DEPT PEDIAT & COMMUNICABLE DIS,D1109 MPB BOX 0718,ANN ARBOR,MI 48109
BIESECKER, LG
.
JOURNAL OF MEDICAL GENETICS,
1993,
30
(07)
:610
-612
←
1
2
3
→
共 22 条
[11]
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome
[J].
Howard, TD
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Howard, TD
;
Paznekas, WA
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Paznekas, WA
;
Green, ED
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Green, ED
;
Chiang, LC
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Chiang, LC
;
Ma, N
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Ma, N
;
DeLuna, RIO
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
DeLuna, RIO
;
Delgado, CG
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Delgado, CG
;
GonzalezRamos, M
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
GonzalezRamos, M
;
Kline, AD
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Kline, AD
;
Jabs, EW
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,CTR MED GENET,BALTIMORE,MD 21287
Jabs, EW
.
NATURE GENETICS,
1997,
15
(01)
:36
-41
[12]
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1
[J].
Johnson, D
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Johnson, D
;
Horsley, SW
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Horsley, SW
;
Moloney, DM
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Moloney, DM
;
Oldridge, M
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Oldridge, M
;
Twigg, SRF
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Twigg, SRF
;
Walsh, S
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Walsh, S
;
Barrow, M
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Barrow, M
;
Njolstad, PR
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Njolstad, PR
;
Kunz, J
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Kunz, J
;
Ashworth, GJ
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Ashworth, GJ
;
Wall, SA
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Wall, SA
;
Kearney, L
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Kearney, L
;
Wilkie, AOM
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
Wilkie, AOM
.
AMERICAN JOURNAL OF HUMAN GENETICS,
1998,
63
(05)
:1282
-1293
[13]
DEFINITION OF THE BLEPHAROPHIMOSIS, PTOSIS, EPICANTHUS INVERSUS SYNDROME CRITICAL REGION AT CHROMOSOME 3Q23 BASED ON THE ANALYSIS OF CHROMOSOMAL-ANOMALIES
[J].
LAWSON, CT
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
LAWSON, CT
;
TOOMES, C
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
TOOMES, C
;
FRYER, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
FRYER, A
;
CARETTE, MJM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
CARETTE, MJM
;
TAYLOR, GM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
TAYLOR, GM
;
FUKUSHIMA, Y
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
FUKUSHIMA, Y
;
DIXON, MJ
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
DIXON, MJ
.
HUMAN MOLECULAR GENETICS,
1995,
4
(05)
:963
-967
[14]
Linkage of blepharophimosis syndrome in a large Indian pedigree to chromosome 7p
[J].
Maw, M
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Maw, M
;
Kar, B
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Kar, B
;
Biswas, J
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Biswas, J
;
Biswas, P
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Biswas, P
;
Nancarrow, D
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Nancarrow, D
;
Bridges, R
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Bridges, R
;
Kumaramanickavel, G
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Kumaramanickavel, G
;
Denton, M
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Denton, M
;
Badrinath, SS
论文数:
0
引用数:
0
h-index:
0
机构:
DEPT MOL BIOL & GENET,MADRAS,TAMIL NADU,INDIA
Badrinath, SS
.
HUMAN MOLECULAR GENETICS,
1996,
5
(12)
:2049
-2054
[15]
Pantke O A, 1975, Birth Defects Orig Artic Ser, V11, P190
[16]
SAETHRE-CHOTZEN SYNDROME
[J].
REARDON, W
论文数:
0
引用数:
0
h-index:
0
REARDON, W
;
WINTER, RM
论文数:
0
引用数:
0
h-index:
0
WINTER, RM
.
JOURNAL OF MEDICAL GENETICS,
1994,
31
(05)
:393
-396
[17]
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases
[J].
Rose, CSP
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Rose, CSP
;
Patel, P
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Patel, P
;
Reardon, W
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Reardon, W
;
Malcolm, S
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Malcolm, S
;
Winter, RM
论文数:
0
引用数:
0
h-index:
0
机构:
INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
Winter, RM
.
HUMAN MOLECULAR GENETICS,
1997,
6
(08)
:1369
-1373
[18]
BLEPHAROPHIMOSIS SYNDROME IS LINKED TO CHROMOSOME 3Q
[J].
SMALL, KW
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
SMALL, KW
;
STALVEY, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
STALVEY, M
;
FISHER, L
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
FISHER, L
;
MULLEN, L
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
MULLEN, L
;
DICKEL, C
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
DICKEL, C
;
BEADLES, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
BEADLES, K
;
REIMER, R
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
REIMER, R
;
LESSNER, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
LESSNER, A
;
LEWIS, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
LEWIS, K
;
PERICAKVANCE, MA
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV FLORIDA, DEPT OPHTHALMOL, GAINESVILLE, FL USA
PERICAKVANCE, MA
.
HUMAN MOLECULAR GENETICS,
1995,
4
(03)
:443
-448
[19]
BLEPHAROPHIMOSIS, PTOSIS, EPICANTHUS INVERSUS, AND PRIMARY AMENORRHEA - DOMINANT TRAIT
[J].
TOWNES, PL
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ROCHESTER,MED CTR,DEPT OBSTET & GYNECOL,ROCHESTER,NY 14627
UNIV ROCHESTER,MED CTR,DEPT OBSTET & GYNECOL,ROCHESTER,NY 14627
TOWNES, PL
;
MUECHLER, EK
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ROCHESTER,MED CTR,DEPT OBSTET & GYNECOL,ROCHESTER,NY 14627
UNIV ROCHESTER,MED CTR,DEPT OBSTET & GYNECOL,ROCHESTER,NY 14627
MUECHLER, EK
.
ARCHIVES OF OPHTHALMOLOGY,
1979,
97
(09)
:1664
-1666
[20]
MILD PHENOTYPIC MANIFESTATION OF A 7P15.3P21.2 DELETION
[J].
WANG, C
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MICHIGAN HOSP,DEPT PEDIAT & COMMUNICABLE DIS,D1109 MPB BOX 0718,ANN ARBOR,MI 48109
WANG, C
;
MAYNARD, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MICHIGAN HOSP,DEPT PEDIAT & COMMUNICABLE DIS,D1109 MPB BOX 0718,ANN ARBOR,MI 48109
MAYNARD, S
;
GLOVER, TW
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MICHIGAN HOSP,DEPT PEDIAT & COMMUNICABLE DIS,D1109 MPB BOX 0718,ANN ARBOR,MI 48109
GLOVER, TW
;
BIESECKER, LG
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MICHIGAN HOSP,DEPT PEDIAT & COMMUNICABLE DIS,D1109 MPB BOX 0718,ANN ARBOR,MI 48109
BIESECKER, LG
.
JOURNAL OF MEDICAL GENETICS,
1993,
30
(07)
:610
-612
←
1
2
3
→