Patient with a deletion of chromosome 21q and minimal phenotype

被引：6

作者：

Tinkel-Vernon, H

Finkernagel, S

Desposito, F

Pittore, C

Reynolds, K

Sciorra, L

机构：

[1] Univ Med & Dent New Jersey, RWJUH, Dept Obstet & Gynecol, New Brunswick, NJ USA

[2] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Pediat, Newark, NJ 07103 USA

[3] Mercer Med Ctr, Capital Hlth Syst, Div Maternal Fetal Med, Trenton, NJ USA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2003年 / 120A卷 / 01期

关键词：

D O I：

10.1002/ajmg.a.10210

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：142 / 143

页数：2

共 9 条

[1]

Ahlbom BE, 1996, AM J MED GENET, V64, P501

[2]

EPSTEIN CJ, 1990, AM J MED GENET, P31

[3] Clonability and gene distribution on human chromosome 21: reflections of junk DNA content? [J].

Gardiner, K .

GENE, 1997, 205 (1-2) :39-46

[4] YAC analysis and minimal tiling path construction for chromosome 21q [J].

Gardiner, K ;

Graw, S ;

Ichikawa, H ;

Ohki, M ;

Joetham, A ;

Gervy, P ;

Chumakov, I ;

Patterson, D .

SOMATIC CELL AND MOLECULAR GENETICS, 1995, 21 (06) :399-414

[5] Bacterial contig map of the 21q11 region associated with Alzheimer's disease and abnormal myelopoiesis in Down syndrome [J].

Groet, J ;

Ives, JH ;

South, AP ;

Baptista, PR ;

Jones, TA ;

Yaspo, ML ;

Lehrach, H ;

Potier, MC ;

Van Broeckhoven, C ;

Nizetic, D .

GENOME RESEARCH, 1998, 8 (04) :385-398

[6] DELETION OF CHROMOSOME-21 AND NORMAL INTELLIGENCE - MOLECULAR DEFINITION OF THE LESION [J].

KORENBERG, JR ;

KALOUSEK, DK ;

ANNEREN, G ;

PULST, SM ;

HALL, JG ;

EPSTEIN, CJ ;

COX, DR .

HUMAN GENETICS, 1991, 87 (02) :112-118

[7]

ROLAND B, 1990, CLIN GENET, V37, P423

[8]

ROONEY DE, 1979, HUMAN CYTOGENETICS P, P39

[9] Gene identification and DNA sequence analysis in the GC-poor 20 megabase region of human chromosome 21 [J].

Yu, JW ;

Tong, SH ;

Shen, YP ;

Kao, FT .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) :6862-6867

← 1 →