FINE MAPPING OF THE HUMAN BONE MORPHOGENETIC PROTEIN-4 GENE (BMP4) TO CHROMOSOME 14Q22-Q23 BY IN-SITU HYBRIDIZATION

被引：25

作者：

VANDENWIJNGAARD, A ^{[1
]}

WEGHUIS, DO ^{[1
]}

BOERSMA, CJC ^{[1
]}

VANZOELEN, EJJ ^{[1
]}

VANKESSEL, AG ^{[1
]}

OLIJVE, W ^{[1
]}

机构：

[1] UNIV NIJMEGEN HOSP,DEPT HUMAN GENET,6500 HB NIJMEGEN,NETHERLANDS

来源：

GENOMICS | 1995年 / 27卷 / 03期

关键词：

D O I：

10.1006/geno.1995.1096

中图分类号：

Q81 [生物工程学（生物技术）]; Q93 [微生物学];

学科分类号：

071005 ; 0836 ; 090102 ; 100705 ;

摘要：

[No abstract available]

引用

页码：559 / 560

页数：2

共 10 条

[1]

[Anonymous], 1994, MENDELIAN INHERITANC

[2]

BRAULKE I, 1991, CLIN GENET, V39, P241

[3] TRANSFORMING GROWTH-FACTOR-BETA GENE FAMILY MEMBERS AND BONE [J].

CENTRELLA, M ;

HOROWITZ, MC ;

WOZNEY, JM ;

MCCARTHY, TL .

ENDOCRINE REVIEWS, 1994, 15 (01) :27-39

[4]

FRANCIS PH, 1994, DEVELOPMENT, V120, P209

[5]

JONES CM, 1991, DEVELOPMENT, V111, P531

[6] FINE MAPPING OF THE HUMAN RECEPTOR-LIKE PROTEIN-TYROSINE-PHOSPHATASE GENE (PTPRM) TO 18P11.2 BY FLUORESCENCE IN-SITU HYBRIDIZATION [J].

SUIJKERBUIJK, RF ;

GEBBINK, MFGB ;

MOOLENAAR, WH ;

VANKESSEL, AG .

CYTOGENETICS AND CELL GENETICS, 1993, 64 (3-4) :245-246

[7]

TABAS JA, 1993, CLIN ORTHOP RELAT R, V293, P310

[8] HOLT-GRAM SYNDROME IS A GENETICALLY HETEROGENEOUS DISEASE WITH ONE LOCUS MAPPING TO HUMAN-CHROMOSOME 12Q [J].

TERRETT, JA ;

NEWBURYECOB, R ;

CROSS, GS ;

FENTON, I ;

RAEBURN, JA ;

YOUNG, ID ;

BROOK, JD .

NATURE GENETICS, 1994, 6 (04) :401-404

[9]

TURLEAU C, 1984, ANN GENET-PARIS, V27, P237

[10] BONE MORPHOGENETIC PROTEINS (BMPS) - THERAPEUTIC POTENTIAL IN HEALING BONY DEFECTS [J].

WANG, EA .

TRENDS IN BIOTECHNOLOGY, 1993, 11 (09) :379-383

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