The origin of genetic defects in the human and their detection in the preimplantation embryo

被引：97

作者：

Delhanty, JDA ^{[1
]}

Handyside, AH ^{[1
]}

机构：

[1] HAMMERSMITH HOSP, ROYAL POSTGRAD MED SCH, INST OBSTET & GYNAECOL, LONDON, ENGLAND

来源：

HUMAN REPRODUCTION UPDATE | 1995年 / 1卷 / 03期

基金：

英国惠康基金;

关键词：

D O I：

10.1093/humupd/1.3.201

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

[No abstract available]

引用

页码：201 / 215

页数：15

共 59 条

[1] 1ST MEIOTIC DIVISION ABNORMALITIES IN HUMAN OOCYTES - MECHANISM OF TRISOMY FORMATION [J].

ANGELL, RR ;

XIAN, J ;

KEITH, J ;

LEDGER, W ;

BAIRD, DT .

CYTOGENETICS AND CELL GENETICS, 1994, 65 (03) :194-202

[2] MITOTIC ERRORS IN SOMATIC-CELLS CAUSE TRISOMY-21 IN ABOUT 4.5-PERCENT OF CASES AND ARE NOT ASSOCIATED WITH ADVANCED MATERNAL AGE [J].

ANTONARAKIS, SE ;

AVRAMOPOULOS, D ;

BLOUIN, JL ;

TALBOT, CC ;

SCHINZEL, AA .

NATURE GENETICS, 1993, 3 (02) :146-150

[3] PARENTAL ORIGIN OF THE EXTRA CHROMOSOME IN TRISOMY-21 AS INDICATED BY ANALYSIS OF DNA POLYMORPHISMS [J].

ANTONARAKIS, SE .

NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (13) :872-876

[4]

ANTONARAKIS SE, 1992, AM J HUM GENET, V50, P544

[5] ON THE PARENTAL ORIGIN OF DENOVO MUTATION IN MAN [J].

CHANDLEY, AC .

JOURNAL OF MEDICAL GENETICS, 1991, 28 (04) :217-223

[6] PREIMPLANTATION PREVENTION OF X-LINKED DISEASE - RELIABLE AND RAPID SEX DETERMINATION OF SINGLE HUMAN-CELLS BY RESTRICTION ANALYSIS OF SIMULTANEOUSLY AMPLIFIED ZFX AND ZFY SEQUENCES [J].

CHONG, SS ;

KRISTJANSSON, K ;

COTA, J ;

HANDYSIDE, AH ;

HUGHES, MR .

HUMAN MOLECULAR GENETICS, 1993, 2 (08) :1187-1191

[7] RAPID METAPHASE AND INTERPHASE DETECTION OF RADIATION-INDUCED CHROMOSOME-ABERRATIONS IN HUMAN-LYMPHOCYTES BY CHROMOSOMAL SUPPRESSION INSITU HYBRIDIZATION [J].

CREMER, T ;

POPP, S ;

EMMERICH, P ;

LICHTER, P ;

CREMER, C .

CYTOMETRY, 1990, 11 (01) :110-118

[8] DETECTION OF ANEUPLOIDY AND CHROMOSOMAL MOSAICISM IN HUMAN EMBRYOS DURING PREIMPLANTATION SEX DETERMINATION BY FLUORESCENT IN-SITU HYBRIDIZATION, (FISH) [J].

DELHANTY, JDA ;

GRIFFIN, DK ;

HANDYSIDE, AH ;

HARPER, J ;

ATKINSON, GHG ;

PIETERS, MHEC ;

WINSTON, RML .

HUMAN MOLECULAR GENETICS, 1993, 2 (08) :1183-1185

[9]

EIBEN B, 1990, AM J HUM GENET, V47, P656

[10]

FISHER JM, 1993, AM J HUM GENET, V52, P1139

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