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Autosomal Dominant Inheritance of Aplasia Cutis Congenita and Congenital Heart Defect: A Possible Link to the Adams-Oliver Syndrome
被引:11
作者
:
Digilio, M. C.
论文数:
0
引用数:
0
h-index:
0
机构:
Bambino Gesu Pediat Hosp, I-00165 Rome, Italy
Bambino Gesu Pediat Hosp, I-00165 Rome, Italy
Digilio, M. C.
[
1
]
Marino, Bruno
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Roma La Sapienza, Dept Pediat, Rome, Italy
Bambino Gesu Pediat Hosp, I-00165 Rome, Italy
Marino, Bruno
[
2
]
Dallapiccola, Bruno
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Roma La Sapienza, Dept Expt Med, Rome, Italy
Bambino Gesu Pediat Hosp, I-00165 Rome, Italy
Dallapiccola, Bruno
[
3
]
机构
:
[1]
Bambino Gesu Pediat Hosp, I-00165 Rome, Italy
[2]
Univ Roma La Sapienza, Dept Pediat, Rome, Italy
[3]
Univ Roma La Sapienza, Dept Expt Med, Rome, Italy
来源
:
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
|
2008年
/ 146A卷
/ 21期
关键词
:
D O I
:
10.1002/ajmg.a.32526
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
引用
收藏
页码:2842 / 2844
页数:3
相关论文
共 25 条
[21]
2-M
[22]
Adams-Oliver syndrome: Further evidence of an autosomal recessive variant
[J].
Temtamy, Samia A.
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Temtamy, Samia A.
;
Aglan, Mona S.
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Aglan, Mona S.
;
Ashour, Adel M.
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Ashour, Adel M.
;
Zaki, Maha S.
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Zaki, Maha S.
.
CLINICAL DYSMORPHOLOGY,
2007,
16
(03)
:141
-149
[23]
Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes
[J].
论文数:
引用数:
h-index:
机构:
Verdyck, P
;
论文数:
引用数:
h-index:
机构:
Blaumeiser, B
;
Holder-Espinasse, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Instelling Antwerp, Dept Med Genet, B-2610 Antwerp, Belgium
Holder-Espinasse, M
;
Van Hul, W
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Instelling Antwerp, Dept Med Genet, B-2610 Antwerp, Belgium
Van Hul, W
;
论文数:
引用数:
h-index:
机构:
Wuyts, W
.
CLINICAL GENETICS,
2006,
69
(01)
:86
-92
[24]
Clinical and molecular analysis of nine families with Adams-Oliver syndrome
[J].
Verdyck, P
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium
Verdyck, P
;
Holder-Espinasse, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium
Holder-Espinasse, M
;
Van Hul, W
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium
Van Hul, W
;
论文数:
引用数:
h-index:
机构:
Wuyts, W
.
EUROPEAN JOURNAL OF HUMAN GENETICS,
2003,
11
(06)
:457
-463
[25]
ZAPATA HH, 1995, CLIN GENET, V47, P80
←
1
2
3
→
共 25 条
[21]
2-M
[22]
Adams-Oliver syndrome: Further evidence of an autosomal recessive variant
[J].
Temtamy, Samia A.
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Temtamy, Samia A.
;
Aglan, Mona S.
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Aglan, Mona S.
;
Ashour, Adel M.
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Ashour, Adel M.
;
Zaki, Maha S.
论文数:
0
引用数:
0
h-index:
0
机构:
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Natl Res Ctr, Dept Clin Genet, Div Human Genet & Genome Res, Cairo, Egypt
Zaki, Maha S.
.
CLINICAL DYSMORPHOLOGY,
2007,
16
(03)
:141
-149
[23]
Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes
[J].
论文数:
引用数:
h-index:
机构:
Verdyck, P
;
论文数:
引用数:
h-index:
机构:
Blaumeiser, B
;
Holder-Espinasse, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Instelling Antwerp, Dept Med Genet, B-2610 Antwerp, Belgium
Holder-Espinasse, M
;
Van Hul, W
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Instelling Antwerp, Dept Med Genet, B-2610 Antwerp, Belgium
Van Hul, W
;
论文数:
引用数:
h-index:
机构:
Wuyts, W
.
CLINICAL GENETICS,
2006,
69
(01)
:86
-92
[24]
Clinical and molecular analysis of nine families with Adams-Oliver syndrome
[J].
Verdyck, P
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium
Verdyck, P
;
Holder-Espinasse, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium
Holder-Espinasse, M
;
Van Hul, W
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Antwerp, Dept Med Genet, B-2610 Wilrijk, Belgium
Van Hul, W
;
论文数:
引用数:
h-index:
机构:
Wuyts, W
.
EUROPEAN JOURNAL OF HUMAN GENETICS,
2003,
11
(06)
:457
-463
[25]
ZAPATA HH, 1995, CLIN GENET, V47, P80
←
1
2
3
→