FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN 3 CHROMOSOMES

被引：21

作者：

CREASY, MR ^{[1
]}

CROLLA, JA ^{[1
]}

DAKER, MG ^{[1
]}

机构：

[1] GUYS HOSP,MED SCH,PAEDIAT RES UNIT,LONDON SE1 9RT,ENGLAND

来源：

HUMANGENETIK | 1974年 / 24卷 / 04期

关键词：

D O I：

10.1007/BF00297594

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：303 / 308

页数：6

共 10 条

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[2] LOCALIZATION OF HETEROCHROMATIN IN HUMAN CHROMOSOMES
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[J]. CYTOGENETICS, 1971, 10 (02): : 81 - &
[3] A COMPLEX FAMILIAL TRANSLOCATION INVOLVING CHROMOSOMES 5,9 AND 13
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HALL, B
[J]. CYTOGENETICS, 1970, 9 (04): : 294 - &
[4] Hamerton JL, 1971, HUMAN CYTOGENETICS, V1
[5] FAMILY WITH 2 TRANSLOCATIONS AND A POLYMORPHISM INVOLVING CHROMOSOME-14
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BUCKTON, KE
CHRISTIE, S
NEWTON, M
MATTHEW, D
[J]. JOURNAL OF MEDICAL GENETICS, 1974, 11 (01) : 65 - 68
[6] JACOBS PA, 1970, INHERITANCE RANDOMLY, P90
[7] A CASE OF MULTIPLE CHROMOSOMAL REARRANGEMENTS WITH PERSISTENCE OF FOETAL HAEMOGLOBIN
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DECARLI, L
SERENI, LP
[J]. CYTOGENETICS, 1968, 7 (03): : 169 - &
[8] PARTIAL TRISOMY 11 IN A CHILD RESULTING FROM A COMPLEX MATERNAL REARRANGEMENT OF CHROMOSOMES 11, 12 AND 13
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YUNIS, JJ
ESCOBAR, JI
[J]. HUMANGENETIK, 1974, 22 (01): : 59 - 65
[9] SEABRIGH.M, 1971, LANCET, V2, P971
[10] 1972, BIRTH DEFECTS OAS, V8, P7