TRANSLOCATION BREAKPOINT IN AARSKOG SYNDROME MAPS TO XP11.21 BETWEEN ALAS2 AND DXS323

被引：12

作者：

GLOVER, TW

VERGA, V

RAFAEL, J

BARCROFT, C

GORSKI, JL

BAWLE, EV

HIGGINS, JV

机构：

[1] MICHIGAN STATE UNIV,DEPT PEDIAT & HUMAN DEV,E LANSING,MI 48824

[2] UNIV MICHIGAN,DEPT PEDIAT,ANN ARBOR,MI 48109

[3] DETROIT CHILDRENS HOSP,DEPT GENET & METAB DISORDERS,DETROIT,MI

来源：

HUMAN MOLECULAR GENETICS | 1993年 / 2卷 / 10期

关键词：

D O I：

10.1093/hmg/2.10.1717

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

[No abstract available]

引用

页码：1717 / 1718

页数：2

共 20 条

[1] A FAMILIAL SYNDROME OF SHORT STATURE ASSOCIATED WITH FACIAL DYSPLASIA AND GENITAL ANOMALIES [J].

AARSKOG, D .

JOURNAL OF PEDIATRICS, 1970, 77 (05) :856-+

[2] AARSKOG SYNDROME - FULL MALE AND FEMALE EXPRESSION ASSOCIATED WITH AN X-AUTOSOME TRANSLOCATION [J].

BAWLE, E ;

TYRKUS, M ;

LIPMAN, S ;

BOZIMOWSKI, D .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 17 (03) :595-602

[3] ENZYMATIC DEFECT IN X-LINKED SIDEROBLASTIC ANEMIA - MOLECULAR EVIDENCE FOR ERYTHROID DELTA-AMINOLEVULINATE SYNTHASE DEFICIENCY [J].

COTTER, PD ;

BAUMANN, M ;

BISHOP, DF .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (09) :4028-4032

[4] ASSIGNMENT OF HUMAN ERYTHROID DELTA-AMINOLEVULINATE SYNTHASE (ALAS2) TO A DISTAL SUBREGION OF BAND XP11.21 BY PCR ANALYSIS OF SOMATIC-CELL HYBRIDS CONTAINING X - AUTOSOME TRANSLOCATIONS [J].

COTTER, PD ;

WILLARD, HF ;

GORSKI, JL ;

BISHOP, DF .

GENOMICS, 1992, 13 (01) :211-212

[5]

COX T, 1992, HUM MOL GENET, V8, P639

[6] REPORT OF THE COMMITTEE-ON-THE-GENETIC-CONSTITUTION-OF-THE-X-CHROMOSOME [J].

DAVIES, KE ;

MANDEL, JL ;

MONACO, AP ;

NUSSBAUM, RL ;

WILLARD, HF .

CYTOGENETICS AND CELL GENETICS, 1991, 58 (1-2) :853-966

[7] AARSKOG SYNDROME - NEW FINDINGS AND GENETIC-ANALYSIS [J].

ESCOBAR, V ;

WEAVER, DD .

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1978, 240 (24) :2638-2641

[8] AARSKOG SYNDROME [J].

FRYNS, JP ;

MACKEN, J ;

VINKEN, L ;

IGODTAMEYE, L ;

VANDENBERGHE, H .

HUMAN GENETICS, 1978, 42 (02) :129-135

[9] A RADIATION HYBRID MAP OF THE PROXIMAL SHORT ARM OF THE HUMAN X-CHROMOSOME SPANNING INCONTINENTIA-PIGMENTI-1 (IP1) TRANSLOCATION BREAKPOINTS [J].

GORSKI, JL ;

BOEHNKE, M ;

REYNER, EL ;

BURRIGHT, EN .

GENOMICS, 1992, 14 (03) :657-665

[10] ISOLATION OF DNA MARKERS FROM A REGION BETWEEN INCONTINENTIA-PIGMENTI-1 (IP1) X-CHROMOSOMAL TRANSLOCATION BREAKPOINTS BY A COMPARATIVE PCR ANALYSIS OF A RADIATION HYBRID SUBCLONE MAPPING PANEL [J].

GORSKI, JL ;

BURRIGHT, EN ;

REYNER, EL ;

GOODFELLOW, PN ;

BURGESS, DL .

GENOMICS, 1992, 14 (03) :649-656

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