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An in situ hybridization-based strategy to detect neuronal patterns of genomic imprinting in the autism candidate region of chromosome 15q11-q13.
被引:0
|
作者
:
Kesterson, RA
论文数:
0
引用数:
0
h-index:
0
机构:
Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
Kesterson, RA
Nurmi, EL
论文数:
0
引用数:
0
h-index:
0
机构:
Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
Nurmi, EL
Johnson, DK
论文数:
0
引用数:
0
h-index:
0
机构:
Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
Johnson, DK
Sutcliffe, JS
论文数:
0
引用数:
0
h-index:
0
机构:
Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
Sutcliffe, JS
机构
:
[1]
Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[2]
Oak Ridge Natl Lab, Mammalian Genet & Dev Sect, Oak Ridge, TN USA
来源
:
AMERICAN JOURNAL OF HUMAN GENETICS
|
2000年
/ 67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
:
873
引用
收藏
页码:165 / 165
页数:1
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[32]
DIFFERENCE IN METHYLATION PATTERNS WITHIN THE D15S9 REGION OF CHROMOSOME 15Q11-13 IN 1ST COUSINS WITH ANGELMAN SYNDROME AND PRADER-WILLI-SYNDROME
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[33]
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[34]
Cryptic t(12;15)(p13;q26) producing the ETV6-NTRK3 fusion gene and no loss of IGF2 imprinting in congenital mesoblastic nephroma with trisomy 11:: fluorescence in situ hybridization and IGF2 allelic expression analysis
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