A transmitted deletion of 2q13 to 2q14.1 causes no phenotypic abnormalities

被引:19
作者
Sumption, ND [1 ]
Barber, JCK [1 ]
机构
[1] Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
关键词
D O I
10.1136/jmg.38.2.125
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:125 / 126
页数:2
相关论文
共 17 条
[1]   DENOVO INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-2 IN A MALFORMED NEWBORN WITH KARYOTYPE - 46,XY,DEL(2)(Q12Q14) [J].
ANTICH, J ;
CARBONELL, X ;
MAS, J ;
CLUSELLAS, N .
ACTA PAEDIATRICA SCANDINAVICA, 1983, 72 (04) :631-633
[2]   Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level [J].
Barber, JCK ;
Reed, CJ ;
Dahoun, SP ;
Joyce, CA .
HUMAN GENETICS, 1999, 104 (03) :211-218
[3]   INTERSTITIAL DELETIONS WITHOUT PHENOTYPIC EFFECT - PRENATAL-DIAGNOSIS OF A NEW FAMILY AND BRIEF REVIEW [J].
BARBER, JCK ;
MAHL, H ;
PORTCH, J ;
CRAWFURD, MD .
PRENATAL DIAGNOSIS, 1991, 11 (06) :411-416
[4]   CHROMOSOME IMBALANCE, NORMAL PHENOTYPE, AND IMPRINTING [J].
BORTOTTO, L ;
PIOVAN, E ;
FURLAN, R ;
RIVERA, H ;
ZUFFARDI, O .
JOURNAL OF MEDICAL GENETICS, 1990, 27 (09) :582-587
[5]   DELETION OF BAND 13Q21 IS COMPATIBLE WITH NORMAL PHENOTYPE [J].
COUTURIER, J ;
MORICHONDELVALLEZ, N ;
DUTRILLAUX, B .
HUMAN GENETICS, 1985, 70 (01) :87-91
[6]   INTERSTITIAL DELETION 2Q14Q21 [J].
FRYDMAN, M ;
STEINBERGER, J ;
SHABTAI, F ;
KATZNELSON, MB ;
VARSANO, I .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (04) :476-479
[7]  
Gardner RJM, 1996, CHROMOSOME ABNORMALI
[8]  
KASAI R, 1988, TERATOLOGY, V38, P529
[9]   DE1(3)(P25.3) WITHOUT PHENOTYPIC EFFECT [J].
KNIGHT, LA ;
YONG, MH ;
TAN, M ;
NG, ISL .
JOURNAL OF MEDICAL GENETICS, 1995, 32 (12) :994-995
[10]  
LAMBERT R, 1991, J MED GENET, V18, P62