CONFIRMATORY LINKAGE OF HYPOCHONDROPLASIA TO CHROMOSOME ARM 4P

被引：7

作者：

HECHT, JT

HERRERA, CA

GREENHAW, GA

FRANCOMANO, CA

BELLUS, GA

BLANTON, SH

机构：

[1] NIH,MED GENET BRANCH,NATL CTR GENOM RES,BETHESDA,MD 20892

[2] JOHNS HOPKINS UNIV,SCH MED,CTR MED GENET,BALTIMORE,MD 21205

[3] UNIV VIRGINIA,DEPT PEDIAT,CHARLOTTESVILLE,VA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 57卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320570333

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：505 / 506

页数：2

共 13 条

[1]

BELLUS GA, 1995, AM J HUM GENET, V56, P368

[2] LOCALIZATION OF THE ACHONDROPLASIA GENE TO THE DISTAL 2.5 MB OF HUMAN-CHROMOSOME-4P [J].

FRANCOMANO, CA ;

DELUNA, RIO ;

HEFFERON, TW ;

BELLUS, GA ;

TURNER, CE ;

TAYLOR, E ;

MEYERS, DA ;

BLANTON, SH ;

MURRAY, JC ;

MCINTOSH, I ;

HECHT, JT .

HUMAN MOLECULAR GENETICS, 1994, 3 (05) :787-792

[3]

FRYMAN M, 1974, CLIN GENET, V5, P223

[4] LINKAGE OF TYPICAL PSEUDOACHONDROPLASIA TO CHROMOSOME-19 [J].

HECHT, JT ;

FRANCOMANO, CA ;

BRIGGS, MD ;

DEERE, M ;

CONNER, B ;

HORTON, WA ;

WARMAN, M ;

COHN, DH ;

BLANTON, SH .

GENOMICS, 1993, 18 (03) :661-666

[5] RADIOGRAPHIC MANIFESTATIONS OF HYPOCHONDROPLASIA [J].

HESELSON, NG ;

CREMIN, BJ ;

BEIGHTON, P .

CLINICAL RADIOLOGY, 1979, 30 (01) :79-85

[6]

LEMERRER M, 1994, NAT GENET, V6, P318

[7]

MCKUSICK VA, 1973, J MED GENET, V10, P11, DOI 10.1136/jmg.10.1.11

[8]

OTT J, 1991, ANAL HUMAN GENETIC L

[9] MUTATIONS IN THE TRANSMEMBRANE DOMAIN OF FGFR3 CAUSE THE MOST COMMON GENETIC FORM OF DWARFISM, ACHONDROPLASIA [J].

SHIANG, R ;

THOMPSON, LM ;

ZHU, YZ ;

CHURCH, DM ;

FIELDER, TJ ;

BOCIAN, M ;

WINOKUR, ST ;

WASMUTH, JJ .

CELL, 1994, 78 (02) :335-342

[10] ACHONDROPLASIA-HYPOCHONDROPLASIA COMPLEX [J].

SOMMER, A ;

YOUNGWEE, T ;

FRYE, T .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 26 (04) :949-957

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