A REVIEW OF PHENOTYPE-KARYOTYPE CORRELATIONS IN INDIVIDUALS WITH INTERSTITIAL DELETIONS OF THE LONG ARM OF CHROMOSOME-2

被引：43

作者：

RAMER, JC ^{[1
]}

LADDA, RL ^{[1
]}

FRANKEL, CA ^{[1
]}

BECKFORD, A ^{[1
]}

机构：

[1] PENN STATE UNIV,MILTON S HERSHEY MED CTR,COLL MED,DEPT OPHTHALMOL,HERSHEY,PA 17033

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1989年 / 32卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320320318

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：359 / 363

页数：5

共 14 条

[1] INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-2 - DEL(2)(Q31Q33) [J].

ALAWADI, SA ;

FARAG, TI ;

NAGUIB, K ;

TEEBI, A ;

CUSCHIERI, A ;

ALOTHMAN, S ;

SUNDARESHAN, TS .

JOURNAL OF MEDICAL GENETICS, 1983, 20 (06) :464-465

[2]

ANTICH J, 1981, CLIN GENET, V19, P489

[3] INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 2 IN A MALFORMED INFANT WITH KARYOTYPE 46,XX,DEL(2)(Q31Q33) [J].

BENSON, K ;

GORDON, M ;

WASSMAN, ER ;

TSI, C .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 25 (03) :405-411

[4] INTERSTITIAL DELETION 2Q31-]Q33 [J].

BUCHANAN, PD ;

RHODES, RL ;

STEVENSON, CE .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 15 (01) :121-126

[5] INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-2 (Q31Q33) IN A GIRL WITH MULTIPLE ANOMALIES AND MENTAL-RETARDATION [J].

FRANCESCHINI, P ;

SILENGO, MC ;

DAVI, G ;

BIANCO, R ;

BIAGIOLI, M .

HUMAN GENETICS, 1983, 64 (01) :98-98

[6] INTERSTITIAL DELETION OF LONG ARM OF CHROMOSOME 2 IN A POLYMALFORMED NEWBORN-KARYOTYPE - 46,XX,DEL(2)(Q21-Q24) [J].

FRYNS, JP ;

VANBOSSTRAETEN, B ;

MALBRAIN, H ;

VANDENBERGHE, H .

HUMAN GENETICS, 1977, 39 (02) :233-238

[7] INTERSTITIAL DELETION OF CHROMOSOME-2 [J].

MARKOVIC, S ;

KRSTIC, M ;

SULOVIC, V ;

RADOJKOVIC, Z ;

ADZIC, S .

JOURNAL OF MEDICAL GENETICS, 1985, 22 (02) :154-155

[8] PARTIAL DELETION OF CHROMOSOME-2 MIMICKING A PHENOTYPE OF TRISOMY-18 - CASE-REPORT WITH AUTOPSY [J].

MCCONNELL, TS ;

KORNFELD, M ;

MCCLELLAN, G ;

AASE, J .

HUMAN PATHOLOGY, 1980, 11 (02) :202-205

[9] IDENTICAL MULTIPLE CONGENITAL-ANOMALIES MENTAL-RETARDATION (MCA/MR) SYNDROME DUE TO DEL(2)(Q32) IN 2 SISTERS WITH INTRACHROMOSOMAL INSERTIONAL TRANSLOCATION IN THEIR FATHER [J].

PAI, GS ;

ROGERS, JF ;

SOMMER, A .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (01) :189-195

[10] A CASE OF DELETION 2Q35-]QTER AND A PECULIAR PHENOTYPE [J].

SANCHEZ, JM ;

PANTANO, AM .

JOURNAL OF MEDICAL GENETICS, 1984, 21 (02) :147-149

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