INCIDENTAL DETECTION OF PREMATURE CENTROMERE SEPARATION IN AMNIOCYTES ASSOCIATED WITH A MILD FORM OF ROBERTS SYNDROME

被引：24
作者：
STANLEY, WS
PAI, GS
HORGER, EO
YONGSHAN, Y
MCNEAL, KS
机构：
[1] MED UNIV S CAROLINA,DEPT PEDIAT,CHARLESTON,SC 29425
[2] MED UNIV S CAROLINA,DEPT OBSTET & GYNECOL,CHARLESTON,SC 29425
来源：
PRENATAL DIAGNOSIS | 1988年 / 8卷 / 08期
关键词：
D O I：
10.1002/pd.1970080803
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：565 / 569
页数：5
相关论文
共 7 条
[1]   PREMATURE CENTROMERE DIVISION - MECHANISM OF NONDISJUNCTION CAUSING X-CHROMOSOME ANEUPLOIDY IN SOMATIC-CELLS OF MAN [J].
FITZGERALD, PH ;
PICKERING, AF ;
MERCER, JM ;
MIETHKE, PM .
ANNALS OF HUMAN GENETICS, 1975, 38 (MAY) :417-428
[2]   SC PHOCOMELIA AND ROBERTS SYNDROME - NOSOLOGIC ASPECTS [J].
HERRMANN, J ;
OPITZ, JM .
EUROPEAN JOURNAL OF PEDIATRICS, 1977, 125 (02) :117-134
[3]   CHROMOSOME-STUDIES OF PATIENTS WITH ALZHEIMER-DISEASE [J].
MOORHEAD, PS ;
HEYMAN, A .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (03) :545-556
[4]   SC-PHOCOMELIA SYNDROME, PREMATURE CENTROMERE SEPARATION, AND CONGENITAL CRANIAL NERVE PARALYSIS IN 2 SISTERS, ONE WITH MALIGNANT-MELANOMA [J].
PARRY, DM ;
MULVIHILL, JJ ;
TSAI, S ;
KAISERKUPFER, MI ;
COWAN, JM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 24 (04) :653-672
[5]   A DOMINANTLY INHERITED CYTOGENETIC ANOMALY - A POSSIBLE CELL-DIVISION MUTANT [J].
RUDD, NL ;
TESHIMA, IE ;
MARTIN, RH ;
SISKEN, JE ;
WEKSBERG, R .
HUMAN GENETICS, 1983, 65 (02) :117-121
[6]  
STAMBERG J, 1987, American Journal of Human Genetics, V41, pA85
[7]   ABNORMAL CENTROMERE-CHROMATID APPOSITION (ACCA) AND PETERS ANOMALY [J].
WERTELECKI, W ;
DEV, VG ;
SUPERNEAU, DW .
OPHTHALMIC PAEDIATRICS AND GENETICS, 1985, 6 (1-2) :7-15
1