Genomic imprinting abnormalities: a new potential risk of assisted reproduction

被引：38

作者：

Tesarik, Jan ^{[1
]}

Mendoza, Carmen ^{[1
]}

机构：

[1] Univ Granada, Fac Sci, Div Reprod Biol, Granada 18071, Spain

来源：

MOLECULAR HUMAN REPRODUCTION | 1996年 / 2卷 / 05期

关键词：

D O I：

10.1093/molehr/2.5.295

中图分类号：

Q [生物科学];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

[No abstract available]

引用

页码：295 / 298

页数：4

共 28 条

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[2] Clayton-Smith J., 1992, HUM GENET, V88, P376
[3] GENOMIC IMPRINTING AND GENE ACTIVATION IN CANCER
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[J]. NATURE GENETICS, 1993, 4 (02) : 110 - 113
[4] GENETIC-ANALYSIS OF GENOMIC IMPRINTING - AN IMPRINTOR-1 GENE CONTROLS INACTIVATION OF THE PATERNAL COPY OF THE MOUSE TME LOCUS
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[J]. CELL, 1992, 70 (03) : 443 - 450
[5] PARENTAL GENOMIC IMPRINTING OF THE HUMAN IGF2 GENE
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[J]. NATURE GENETICS, 1993, 4 (01) : 98 - 101
[6] FUNCTIONAL IMPRINTING AND EPIGENETIC MODIFICATION OF THE HUMAN SNRPN GENE
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[J]. HUMAN MOLECULAR GENETICS, 1993, 2 (12) : 2001 - 2005
[7] TUMOR-SUPPRESSOR ACTIVITY OF H19 RNA
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CRENSHAW, T
MOULTON, T
NEWCOMB, E
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[J]. NATURE, 1993, 365 (6448) : 764 - 767
[8] UNIPARENTAL PATERNAL DISOMY IN A GENETIC CANCER-PREDISPOSING SYNDROME
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CHEHENSSE, V
BELDJORD, C
SCHWARTZ, C
UTERMANN, G
JUNIEN, C
[J]. NATURE, 1991, 351 (6328) : 665 - 667
[9] ANGELMAN AND PRADER-WILLI SYNDROMES SHARE A COMMON CHROMOSOME-15 DELETION BUT DIFFER IN PARENTAL ORIGIN OF THE DELETION
KNOLL, JHM
NICHOLLS, RD
MAGENIS, RE
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LALANDE, M
LATT, SA
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (02): : 285 - 290
[10] KOUFOS A, 1989, AM J HUM GENET, V44, P711

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