DEFICIENCY, TRANSPOSITION, AND DUPLICATION OF ONE 15Q REGION MAY BE ALTERNATIVELY ASSOCIATED WITH PRADER-WILLI (OR A SIMILAR) SYNDROME - ANALYSIS OF 7 CASES AFTER VARYING ASCERTAINMENT

被引：48

作者：

FRACCARO, M

ZUFFARDI, O

BUHLER, E

SCHINZEL, A

SIMONI, G

WITKOWSKI, R

BONIFACI, E

CAUFIN, D

CIGNACCO, G

DELENDI, N

GARGANTINI, L

LOSANOWA, T

MARCA, L

ULLRICH, E

VIGI, V

机构：

[1] KINDERSPITAL,BASEL,SWITZERLAND

[2] UNIV ZURICH,INST MED GENET,CH-8006 ZURICH,SWITZERLAND

[3] UNIV MILAN,OSTET CLIN,I-20133 MILAN,ITALY

[4] HUMBOLDT UNIV,BEREICH MED CHARITE,MED GENET ABT,DDR-1040 BERLIN,GER DEM REP

[5] OSPED CIVILE,BELLUNO,ITALY

[6] OSPED CIVILE,PORDENONE,ITALY

[7] UNIV MILAN,PEDIAT CLIN 4,I-20133 MILAN,ITALY

[8] OSPED NIGUARDA,MILANO,ITALY

[9] UNIV FERRARA,IST PUERICULTURA & MED NEONATALE,I-44100 FERRARA,ITALY

来源：

关键词：

D O I：

10.1007/BF00292373

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：388 / 394

页数：7

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