EXPERIENCE WITH FRA(X) (Q27) IN RETARDED MALES AND CARRIER FEMALES

被引：0

作者：

SUTHERLAND, GR ^{[1
]}

机构：

[1] ADELAIDE CHILDRENS HOSP,CYTOGENET UNIT,N ADELAIDE 5006,S AUSTRALIA,AUSTRALIA

来源：

PATHOLOGY | 1980年 / 12卷 / 01期

关键词：

D O I：

10.1016/S0031-3025(16)38607-X

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

引用

页码：141 / 141

页数：1

共 49 条

[21] 在三例杂合子女性中脆性X染色体fra(X)(q27)的复制
施文芳
国外医学遗传学分册, 1983, (06) : 326 - 327
[22] PRENATAL-DIAGNOSIS OF A FETUS WITH AN EXTRA IDIC(X) (Q27)
DALLAPICCOLA, B
FERRANTI, G
PRIMA, L
PRENATAL DIAGNOSIS, 1989, 9 (04) : 293 - 295
[23] TRANSMISSION OF FRAGILE (X)(Q27) FROM NORMAL MALE(S)
FRYNS, JP
VANDENBERGHE, H
HUMAN GENETICS, 1982, 61 (03) : 262 - 263
[24] TRANSMITTING MALES AND CARRIER FEMALES IN FRAGILE-X - REVISITED
LOESCH, DZ
HAY, DA
MULLEY, J
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 51 (04): : 392 - 399
[25] CO-CULTIVATION STUDIES IN THE EXPRESSION OF FRAGILE(X) (Q27) IN LYMPHOCYTES
WEBB, TP
CLINICAL GENETICS, 1985, 27 (06) : 529 - 534
[26] MACRO-ORCHIDISM AND FRAGILE-X IN MENTALLY-RETARDED MALES - CLINICAL, CYTOGENETIC, AND SOME HORMONAL INVESTIGATIONS IN MENTALLY-RETARDED MALES, INCLUDING 2 WITH THE FRAGILE SITE AT XQ28, FRA(X)(Q28)
NIELSEN, KB
TOMMERUP, N
DYGGVE, HV
SCHOU, C
HUMAN GENETICS, 1982, 61 (02) : 113 - 117
[27] THE COMMON FRAGILE SITE IN BAND Q27 OF THE HUMAN X-CHROMOSOME IS NOT COINCIDENT WITH THE FRAGILE-X
SUTHERLAND, GR
BAKER, E
CLINICAL GENETICS, 1990, 37 (03) : 167 - 172
[28] CHARACTERIZATION OF CARRIER FEMALES AND AFFECTED MALES WITH X-LINKED RECESSIVE NEPHROLITHIASIS
REINHART, SC
NORDEN, AGW
LAPSLEY, M
THAKKER, RV
PANG, J
MOSES, AM
FRYMOYER, PA
FAVUS, MJ
HOEPNER, JA
SCHEINMAN, SJ
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 1995, 5 (07): : 1451 - 1461
[29] STUDY OF A LARGE SIBSHIP WITH MENTALLY-RETARDED MALES AND FEMALES CARRYING FRAGILE-X
TEJADA, I
NICOLAS, H
CHERUY, C
BOUE, J
CLINICAL GENETICS, 1983, 23 (03) : 250 - 251
[30] 45，X／46，X，psu　dic（X）（q27）伴原发性闭经一例
施丽华，张宝珍
中华医学遗传学杂志, 1996, (03) : 155 - 155

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