学术探索
学术期刊
新闻热点
数据分析
智能评审
立即登录
UNKNOWN SYNDROME - HOLOPROSENCEPHALY, CONGENITAL HEART-DEFECTS, AND POLYDACTYLY
被引:32
作者
:
YOUNG, ID
论文数:
0
引用数:
0
h-index:
0
机构:
LEICESTER ROYAL INFIRM,DEPT HISTOPATHOL,LEICESTER LE2 7LX,ENGLAND
LEICESTER ROYAL INFIRM,DEPT HISTOPATHOL,LEICESTER LE2 7LX,ENGLAND
YOUNG, ID
[
1
]
MADDERS, DJ
论文数:
0
引用数:
0
h-index:
0
机构:
LEICESTER ROYAL INFIRM,DEPT HISTOPATHOL,LEICESTER LE2 7LX,ENGLAND
LEICESTER ROYAL INFIRM,DEPT HISTOPATHOL,LEICESTER LE2 7LX,ENGLAND
MADDERS, DJ
[
1
]
机构
:
[1]
LEICESTER ROYAL INFIRM,DEPT HISTOPATHOL,LEICESTER LE2 7LX,ENGLAND
来源
:
JOURNAL OF MEDICAL GENETICS
|
1987年
/ 24卷
/ 11期
关键词
:
D O I
:
10.1136/jmg.24.11.714
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
引用
收藏
页码:714 / 715
页数:2
相关论文
共 3 条
[1]
SPECTRUM OF ANOMALIES IN THE MECKEL SYNDROME, OR - MAYBE THERE IS A MALFORMATION SYNDROME WITH AT LEAST ONE CONSTANT ANOMALY
FRASER, FC
论文数:
0
引用数:
0
h-index:
0
机构:
MCGILL UNIV, DEPT PAEDIAT, MONTREAL H3A 1B1, QUEBEC, CANADA
FRASER, FC
LYTWYN, A
论文数:
0
引用数:
0
h-index:
0
机构:
MCGILL UNIV, DEPT PAEDIAT, MONTREAL H3A 1B1, QUEBEC, CANADA
LYTWYN, A
[J].
AMERICAN JOURNAL OF MEDICAL GENETICS,
1981,
9
(01):
: 67
-
73
[2]
SALONEN R, 1981, CLIN GENET, V19, P321
[3]
A COMPUTERIZED DATA-BASE FOR THE DIAGNOSIS OF RARE DYSMORPHIC SYNDROMES
WINTER, RM
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN RES CTR,MRC,DIV INHERITED METAB DIS,HARROW HA1 3UJ,MIDDX,ENGLAND
WINTER, RM
BARAITSER, M
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN RES CTR,MRC,DIV INHERITED METAB DIS,HARROW HA1 3UJ,MIDDX,ENGLAND
BARAITSER, M
DOUGLAS, JM
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN RES CTR,MRC,DIV INHERITED METAB DIS,HARROW HA1 3UJ,MIDDX,ENGLAND
DOUGLAS, JM
[J].
JOURNAL OF MEDICAL GENETICS,
1984,
21
(02)
: 121
-
123
←
1
→
共 3 条
[1]
SPECTRUM OF ANOMALIES IN THE MECKEL SYNDROME, OR - MAYBE THERE IS A MALFORMATION SYNDROME WITH AT LEAST ONE CONSTANT ANOMALY
FRASER, FC
论文数:
0
引用数:
0
h-index:
0
机构:
MCGILL UNIV, DEPT PAEDIAT, MONTREAL H3A 1B1, QUEBEC, CANADA
FRASER, FC
LYTWYN, A
论文数:
0
引用数:
0
h-index:
0
机构:
MCGILL UNIV, DEPT PAEDIAT, MONTREAL H3A 1B1, QUEBEC, CANADA
LYTWYN, A
[J].
AMERICAN JOURNAL OF MEDICAL GENETICS,
1981,
9
(01):
: 67
-
73
[2]
SALONEN R, 1981, CLIN GENET, V19, P321
[3]
A COMPUTERIZED DATA-BASE FOR THE DIAGNOSIS OF RARE DYSMORPHIC SYNDROMES
WINTER, RM
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN RES CTR,MRC,DIV INHERITED METAB DIS,HARROW HA1 3UJ,MIDDX,ENGLAND
WINTER, RM
BARAITSER, M
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN RES CTR,MRC,DIV INHERITED METAB DIS,HARROW HA1 3UJ,MIDDX,ENGLAND
BARAITSER, M
DOUGLAS, JM
论文数:
0
引用数:
0
h-index:
0
机构:
CLIN RES CTR,MRC,DIV INHERITED METAB DIS,HARROW HA1 3UJ,MIDDX,ENGLAND
DOUGLAS, JM
[J].
JOURNAL OF MEDICAL GENETICS,
1984,
21
(02)
: 121
-
123
←
1
→