TRIPLEX GENE DOSAGE EFFECT FOR BETA-GLUCURONIDASE AND POSSIBLE ASSIGNMENT TO BAND Q22 IN A PARTIAL DUPLICATION 7Q

被引：21

作者：

DANESINO, C ^{[1
]}

GIMELLI, G ^{[1
]}

CUOCO, C ^{[1
]}

CICCONE, MO ^{[1
]}

机构：

[1] IST GIANNINA GASLINI,LAB 2,I-16148 GENOA,ITALY

来源：

HUMAN GENETICS | 1981年 / 56卷 / 03期

关键词：

D O I：

10.1007/BF00274695

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

收藏

页码：371 / 373

页数：3

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共 9 条

[1] ARYLSULFATASE B DEFICIENCY IN MAROTEAUX-LAMY SYNDROME - CELLULAR STUDIES AND CARRIER IDENTIFICATION
BERATIS, NG
TURNER, BM
WEISS, R
HIRSCHHORN, K
[J]. PEDIATRIC RESEARCH, 1975, 9 (05) : 475 - 480
[2] BERGER R, 1977, CLIN GENET, V11, P39
[3] DIAGNOSIS OF POMPES DISEASE IN CULTURED SKIN FIBROBLASTS AND PRIMARY AMNIOTIC-FLUID CELLS USING 4-METHYLUMBELLIFERYL-ALPHA-D-GLUCOPYRANOSIDE AS SUBSTRATE
BUTTERWORTH, J
BROADHEAD, DM
[J]. CLINICA CHIMICA ACTA, 1977, 78 (02) : 335 - 342
[4] DUBOSSON J D, 1978, Archiv fuer Genetik, V51, P56
[5] PK-3 - A NEW CHROMOSOME ENZYME MARKER FOR GENE DOSAGE STUDIES IN CHROMOSOME-15 IMBALANCE
JUNIEN, C
RUBINSONSKALA, H
DREYFUS, JC
RAVISE, N
BOUE, J
BOUE, A
KAPLAN, JC
[J]. HUMAN GENETICS, 1980, 54 (02) : 191 - 196
[6] KHAN PM, 1979, CYTOGENET CELL GENET, V25, P39
[7] PARTIAL TRISOMY FOR THE LONG ARM OF CHROMOSOME-7 DUE TO FAMILIAL BALANCED TRANSLOCATION
SCHMID, M
WOLF, J
NESTLER, H
KRONE, W
[J]. HUMAN GENETICS, 1979, 49 (03) : 283 - 289
[8] FULL TRISOMY-7 AND POTTER SYNDROME
YUNIS, E
RAMIREZ, E
URIBE, JG
[J]. HUMAN GENETICS, 1980, 54 (01) : 13 - 18
[9] HIGH-RESOLUTION OF HUMAN CHROMOSOMES
YUNIS, JJ
[J]. SCIENCE, 1976, 191 (4233) : 1268 - 1270