Exclusion of chromosome 7 for Kartagener syndrome but suggestion of linkage in families with other forms of primary ciliary dyskinesia

被引：14

作者：

Witt, M

Wang, YF

Wang, SB

Sun, CE

Pawlik, J

Rutkiewicz, E

Zebrak, J

Diehl, SR ^{[1
]}

机构：

[1] Polish Acad Sci, Inst Human Genet, PL-60479 Poznan, Poland

[2] NIH, Natl Inst Dent & Craniofacial Res, Bethesda, MD 20892 USA

[3] Inst TB & Lung Dis, Rabka, Poland

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 64卷 / 01期

关键词：

D O I：

10.1086/302203

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：313 / 318

页数：6

共 28 条

[1]

Afzelius B., 1995, The Metabolic and Molecular Bases of Inherited Disease, P3943

[2]

AFZELIUS B A, 1976, Science (Washington D C), V193, P317

[3] USHER SYNDROME TYPE-I ASSOCIATED WITH BRONCHIECTASIS AND IMMOTILE NASAL CILIA IN 2 BROTHERS [J].

BONNEAU, D ;

RAYMOND, F ;

KREMER, C ;

KLOSSEK, JM ;

KAPLAN, J ;

PATTE, F .

JOURNAL OF MEDICAL GENETICS, 1993, 30 (03) :253-254

[4] HIGH-SPEED CINEMICROGRAPHIC STUDIES ON RABBIT TRACHEAL (CILIATED) EPITHELIA - CYTOLYTIC EFFECT OF CYSTIC-FIBROSIS SERUM ON TRACHEAL EPITHELIAL-CELLS [J].

CHEUNG, ATW ;

JAHN, TL .

PEDIATRIC RESEARCH, 1976, 10 (02) :144-147

[5] Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32 [J].

Eudy, JD ;

MaEdmonds, M ;

Yao, SF ;

Talmadge, CB ;

Kelley, PM ;

Weston, MD ;

Kimberling, WJ ;

Sumegi, J .

GENOMICS, 1997, 43 (01) :104-106

[6]

GASPARINI P, 1994, HUM GENET, V94, P671

[7] SPLIT HAND SPLIT FOOT ANOMALY IN A FAMILY SEGREGATING A BALANCED TRANSLOCATION WITH BREAKPOINT ON 7Q22.1 [J].

GENUARDI, M ;

POMPONI, MG ;

SAMMITO, V ;

BELLUSSI, A ;

ZOLLINO, M ;

NERI, G .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (06) :823-831

[8]

HANDEL MA, 1985, MOUSE NEWS LETT, V72, P124

[9] Chromosomal mapping of two members of the human dynein gene family to chromosome regions 7p15 and 11q13 near the deafness loci DFNA 5 and DFNA 11 [J].

Kastury, K ;

Taylor, WE ;

Gutierrez, M ;

Ramirez, L ;

Coucke, PJ ;

VanHauwe, P ;

VanCamp, G ;

Bhasin, S .

GENOMICS, 1997, 44 (03) :362-364

[10] HUMAN SITUS DETERMINATION AND CHROMOSOME CONSTITUTION 46,XY,INS(7-8)(Q22-Q12Q24) [J].

KOIFFMANN, CP ;

WAJNTAL, A ;

DESOUZA, DH ;

GONZALEZ, CH ;

COATES, MV .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (04) :568-569

← 1 2 3 →