首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
The recurrent t(11;22): FISH analysis of 11q23 and 22q11 in oogenesis.
被引:0
|
作者
:
Emanuel, BS
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
Emanuel, BS
Conforto, D
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
Conforto, D
Cohen, MM
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
Cohen, MM
机构
:
[1]
Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[2]
Greater Baltimore Med Ctr, Baltimore, MD USA
来源
:
AMERICAN JOURNAL OF HUMAN GENETICS
|
2001年
/ 69卷
/ 04期
关键词
:
D O I
:
暂无
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
204
引用
收藏
页码:216 / 216
页数:1
相关论文
共 50 条
[1]
Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22)
Kurahashi, H
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Kurahashi, H
Shaikh, TH
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Shaikh, TH
Hu, P
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Hu, P
Roe, BA
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Roe, BA
Emanuel, BS
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Emanuel, BS
Budarf, ML
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Budarf, ML
HUMAN MOLECULAR GENETICS,
2000,
9
(11)
: 1665
-
1670
[2]
Tightly clustered 11q23 and 22q11 breakpoints permit PCR based detection of the recurrent constitutional t(11;22).
Kurahashi, H
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Kurahashi, H
Shaikh, TH
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Shaikh, TH
Zackai, EH
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Zackai, EH
Celle, L
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Celle, L
Driscoll, DA
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Driscoll, DA
Budarf, ML
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Budarf, ML
Emanuel, BS
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA
Emanuel, BS
AMERICAN JOURNAL OF HUMAN GENETICS,
2000,
67
(04)
: 146
-
146
[3]
Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22)
Kurahashi, H
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Kurahashi, H
Shaikh, TH
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Shaikh, TH
Zackai, EH
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Zackai, EH
Celle, L
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Celle, L
Driscoll, DA
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Driscoll, DA
Budarf, ML
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Budarf, ML
Emanuel, BS
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
Emanuel, BS
AMERICAN JOURNAL OF HUMAN GENETICS,
2000,
67
(03)
: 763
-
768
[4]
Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families
Shaikh, TH
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Abramson Res Ctr 1002, Philadelphia, PA 19104 USA
Shaikh, TH
Budarf, ML
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Abramson Res Ctr 1002, Philadelphia, PA 19104 USA
Budarf, ML
Celle, L
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Abramson Res Ctr 1002, Philadelphia, PA 19104 USA
Celle, L
Zackai, EH
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Abramson Res Ctr 1002, Philadelphia, PA 19104 USA
Zackai, EH
Emanuel, BS
论文数:
0
引用数:
0
h-index:
0
机构:
Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Abramson Res Ctr 1002, Philadelphia, PA 19104 USA
Emanuel, BS
AMERICAN JOURNAL OF HUMAN GENETICS,
1999,
65
(06)
: 1595
-
1607
[5]
A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation
Edelmann, L
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Edelmann, L
Spiteri, E
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Spiteri, E
McCain, N
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
McCain, N
Goldberg, R
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Goldberg, R
Pandita, RK
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Pandita, RK
Duong, S
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Duong, S
Fox, J
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Fox, J
Blumenthal, D
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Blumenthal, D
Lalani, SR
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Lalani, SR
Shaffer, LG
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Shaffer, LG
Morrow, BE
论文数:
0
引用数:
0
h-index:
0
机构:
Yeshiva Univ Albert Einstein Coll Med, Dept Med Genet, Bronx, NY 10461 USA
Morrow, BE
AMERICAN JOURNAL OF HUMAN GENETICS,
1999,
65
(06)
: 1608
-
1616
[6]
PROGRESS TOWARDS CLONING THE 22Q11 BREAKPOINT OF THE RECURRENT CONSTITUTIONAL T(11-22)
BARNOSKI, BL
论文数:
0
引用数:
0
h-index:
0
机构:
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
BARNOSKI, BL
EMANUEL, BS
论文数:
0
引用数:
0
h-index:
0
机构:
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
EMANUEL, BS
BELL, CJ
论文数:
0
引用数:
0
h-index:
0
机构:
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
BELL, CJ
STRAAKA, M
论文数:
0
引用数:
0
h-index:
0
机构:
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
STRAAKA, M
TATSUMURA, Y
论文数:
0
引用数:
0
h-index:
0
机构:
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
TATSUMURA, Y
BUDARF, ML
论文数:
0
引用数:
0
h-index:
0
机构:
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
CHILDRENS HOSP PHILADELPHIA,PHILADELPHIA,PA 19104
BUDARF, ML
AMERICAN JOURNAL OF HUMAN GENETICS,
1995,
57
(04)
: 594
-
594
[7]
Deletion 22q11
Miller, Simone
论文数:
0
引用数:
0
h-index:
0
机构:
Hannover Med Sch, Klin Phoniatrie & Padaudiol, Hannover, Germany
Hannover Med Sch, Klin Phoniatrie & Padaudiol, Hannover, Germany
Miller, Simone
Ptok, Martin
论文数:
0
引用数:
0
h-index:
0
机构:
Hannover Med Sch, Klin Phoniatrie & Padaudiol, Hannover, Germany
Hannover Med Sch, Klin Phoniatrie & Padaudiol, Hannover, Germany
Ptok, Martin
SPRACHE-STIMME-GEHOR,
2020,
44
(01):
: 58
-
59
[8]
MOLECULAR AND CYTOGENETIC STUDIES OF 22Q11 - THE 11Q22Q TRANSLOCATION
EMANUEL, BS
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,PHILADELPHIA,PA 19104
EMANUEL, BS
SYLVESTER, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,PHILADELPHIA,PA 19104
SYLVESTER, J
ZACKAI, EH
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,PHILADELPHIA,PA 19104
ZACKAI, EH
AMERICAN JOURNAL OF HUMAN GENETICS,
1983,
35
(06)
: A130
-
A130
[9]
Prenatal detection of a deletion 22q11 by FISH
Garcia-Heras, J
论文数:
0
引用数:
0
h-index:
0
机构:
Bur Labs, Genet Testing Ctr, Texas Dept Hlth, Denton, TX 76201 USA
Garcia-Heras, J
Rao, PN
论文数:
0
引用数:
0
h-index:
0
机构:
Bur Labs, Genet Testing Ctr, Texas Dept Hlth, Denton, TX 76201 USA
Rao, PN
Stettler, RW
论文数:
0
引用数:
0
h-index:
0
机构:
Bur Labs, Genet Testing Ctr, Texas Dept Hlth, Denton, TX 76201 USA
Stettler, RW
Huslig, M
论文数:
0
引用数:
0
h-index:
0
机构:
Bur Labs, Genet Testing Ctr, Texas Dept Hlth, Denton, TX 76201 USA
Huslig, M
Smart, RL
论文数:
0
引用数:
0
h-index:
0
机构:
Bur Labs, Genet Testing Ctr, Texas Dept Hlth, Denton, TX 76201 USA
Smart, RL
Pettenati, MJ
论文数:
0
引用数:
0
h-index:
0
机构:
Bur Labs, Genet Testing Ctr, Texas Dept Hlth, Denton, TX 76201 USA
Pettenati, MJ
PRENATAL DIAGNOSIS,
1998,
18
(04)
: 411
-
413
[10]
Neuropathology of 22q11 Deletion Syndrome (22q11DS) in an Infant
论文数:
引用数:
h-index:
机构:
McFadden, Kathryn
Wu, Peter
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pittsburgh, Pittsburgh, PA 15260 USA
Univ Pittsburgh, Pittsburgh, PA 15260 USA
Wu, Peter
Murdoch, Geoffrey
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pittsburgh, Pittsburgh, PA 15260 USA
Univ Pittsburgh, Pittsburgh, PA 15260 USA
Murdoch, Geoffrey
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY,
2012,
71
(06):
: 559
-
559
←
1
2
3
4
5
→