PRENATAL-DIAGNOSIS OF EUCHROMATIC 16P+ HETEROMORPHISMS IN 2 UNRELATED FAMILIES

被引：11

作者：

BOGART, MH

BRADSHAW, C

JONES, OW

机构：

来源：

PRENATAL DIAGNOSIS | 1991年 / 11卷 / 06期

关键词：

D O I：

10.1002/pd.1970110614

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：417 / 418

页数：2

共 10 条

[1] A RARE NON-HETEROCHROMATIC 9P+ VARIANT IN 2 AMNIOTIC-FLUID CELL-CULTURES [J].

ARCHIDIACONO, N ;

PECILE, V ;

ROCCHI, M ;

DALPRA, L ;

NOCERA, G ;

SIMONI, G .

PRENATAL DIAGNOSIS, 1984, 4 (03) :231-233

[2] DUPLICATION OF EUCHROMATIN WITHOUT PHENOTYPIC EFFECTS - A VARIANT OF CHROMOSOME-16 [J].

BRYKE, CR ;

BREG, WR ;

POTLURI, VR ;

YANGFENG, TL .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 36 (01) :43-44

[3]

BUCKTON KE, 1980, ANN HUM GENET, V43, P277

[4]

CLARK RE, 1988, CLIN GENET, V33, P418

[5] EUCHROMATIC 16P+ HETEROMORPHISM - 1ST-REPORT IN NORTH-AMERICA [J].

JALAL, SM ;

SCHNEIDER, NR ;

KUKOLICH, MK ;

WILSON, GN .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1990, 37 (04) :548-550

[6] AN UNUSUAL VARIANT OF CHROMOSOME-16 - 2 NEW CASES [J].

PINEL, I ;

DEBUSTAMANTE, AD ;

URIOSTE, M ;

FELIX, V ;

URETA, A ;

MARTINEZFRIAS, ML .

HUMAN GENETICS, 1988, 80 (02) :194-194

[7]

SPEDICATO FS, 1985, CLIN GENET, V28, P162

[8]

SUTHERLAND GR, 1981, CLIN GENET, V19, P331

[9]

THOMPSON PW, 1987, HUM GENET, V76, P100

[10] NON C-BANDING VARIANTS IN SOME NORMAL-FAMILIES MIGHT BE HOMOGENEOUSLY STAINING REGIONS [J].

WEBB, GC ;

KRUMINS, EJM ;

EICHENBAUM, SZ ;

VOULLAIRE, LE ;

EARLE, E ;

CHOO, KH .

HUMAN GENETICS, 1989, 82 (01) :59-62

← 1 →