HAPLOTYPE DISTRIBUTION AND MOLECULAR DEFECTS OF PKU IN ITALY

被引：3

作者：

DIANZANI, I

CAMASCHELLA, C

SAGLIO, G

FERRERO, GB

ROMEO, G

DEVOTO, M

ROMANO, C

CERONE, R

GIOVANNINI, M

RIVA, E

TREFZ, FK

LICHTERKONECKI, U

WOO, SLC

机构：

[1] UNIV TURIN,DIPARTIMENTO SCI BIOMED & ONCOL UMANA,I-10126 TURIN,ITALY

[2] IST GIANNINA GASLINI,GENET MOLEC LAB,I-16148 GENOA,ITALY

[3] UNIV GENOA,I-16126 GENOA,ITALY

[4] UNIV MILAN,I-20122 MILAN,ITALY

[5] UNIV HEIDELBERG,KINDERKLIN,W-6900 HEIDELBERG,GERMANY

[6] HOWARD HUGHES MED INST,DEPT CELLULAR BIOL & MOLEC GENET,HOUSTON,TX

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1990年 / 13卷 / 03期

关键词：

D O I：

10.1007/BF01799377

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：292 / 294

页数：3

共 9 条

[1] PHENYLKETONURIA - DISTRIBUTION OF DNA DIAGNOSTIC PATTERNS IN GERMAN FAMILIES
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[2] CHAKRABORTY R, 1987, HUM GENET, V76, P40
[3] RFLPS OF THE PHENYLALANINE-HYDROXYLASE GENE IN THE ITALIAN POPULATION
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[5] AN AMINO-ACID SUBSTITUTION INVOLVED IN PHENYLKETONURIA IS IN LINKAGE DISEQUILIBRIUM WITH DNA HAPLOTYPE-2
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[6] TIGHT LINKAGE BETWEEN A SPLICING MUTATION AND A SPECIFIC DNA HAPLOTYPE IN PHENYLKETONURIA
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[7] DNA HAPLOTYPE ANALYSIS AT THE PHENYLALANINE-HYDROXYLASE LOCUS IN THE TURKISH POPULATION
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SCHLOTTER, M
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[J]. HUMAN GENETICS, 1989, 81 (04) : 373 - 376
[8] LINKAGE DISEQUILIBRIUM BETWEEN MUTATION AND RFLP HAPLOTYPE AT THE PHENYLALANINE-HYDROXYLASE LOCUS IN THE GERMAN POPULATION
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SCHLOTTER, M
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[J]. HUMAN GENETICS, 1988, 78 (04) : 347 - 352
[9] MOLECULAR-BASIS AND POPULATION-GENETICS OF PHENYLKETONURIA
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[J]. BIOCHEMISTRY, 1989, 28 (01) : 1 - 7

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