DIAGNOSIS OF CHROMOSOME-3 DUPLICATION Q23-]QTER, DELETION P25-]PTER IN A PATIENT WITH THE C (TRIGONOCEPHALY) SYNDROME

被引：34

作者：

PREUS, M

VEKEMANS, M

KAPLAN, P

机构：

[1] MONTREAL CHILDRENS HOSP,DIV MED GENET,2300 TUPPER ST,MONTREAL H3H 1P3,QUEBEC,CANADA

[2] MEM UNIV NEWFOUNDLAND,FAC MED,ST JOHNS A1C 5S7,NEWFOUNDLAND,CANADA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1986年 / 23卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320230409

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：935 / 943

页数：9

共 21 条

[1]

ALLDERDICE PW, 1975, AM J HUM GENET, V27, P699

[2] FURTHER DELINEATION OF THE C-(TRIGONOCEPHALY) SYNDROME [J].

ANTLEY, RM ;

HWANG, DS ;

THEOPOLD, W ;

GORLIN, RJ ;

STEEPER, T ;

PITT, D ;

DANKS, DM ;

MCPHERSON, E ;

BARTELS, H ;

WIEDEMANN, HR ;

OPITZ, JM .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1981, 9 (02) :147-163

[3] PARTIAL 3Q-TRISOMY DUE TO AN UN-BALANCED 3-10 TRANSLOCATION [J].

BLUMBERG, B ;

MOORE, R ;

MOHANDAS, T .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 7 (03) :335-339

[4]

Boon W H, 1967, J Singapore Paediatr Soc, V9, P88

[5]

CURRY CJR, 1982, BIRTH DEFECTS-ORIG, V18, P275

[6] OPITZ TRIGONOCEPHALY SYNDROME - REPORT OF 2 CASES [J].

FLATZ, SD ;

SCHINZEL, A ;

DOEHRING, E ;

KAMRAN, D ;

EILERS, E .

EUROPEAN JOURNAL OF PEDIATRICS, 1984, 141 (03) :183-185

[7]

Francke U, 1978, Birth Defects Orig Artic Ser, V14, P191

[8] TRIGONOCEPHALY - A NEW FAMILIAL SYNDROME [J].

FRYDMAN, M ;

KAUSCHANSKY, A ;

ELIAN, E .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 18 (01) :55-59

[9] PERICENTRIC INVERSIONS - PROBLEMS AND SIGNIFICANCE FOR CLINICAL GENETICS [J].

KAISER, P .

HUMAN GENETICS, 1984, 68 (01) :1-47

[10]

KRONICK JB, 1983, PEDIATRICS, V71, P960

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