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SAETHRE-CHOTZEN SYNDROME WITH FAMILIAL TRANSLOCATION AT CHROMOSOME 7P22
Author(s): REID CS, MCMORROW LE, MCDONALDMCGINN DM, GRACE KJ, RAMOS FJ, ZACKAI EH, COHEN MM, JABS EW
Source: AMERICAN JOURNAL OF MEDICAL GENETICS    Volume: 47    Issue: 5    Pages: 637-639    Published: OCT 1 1993  
Times Cited: 42     References: 18     
Abstract: Chromosome analysis Of a male infant and his mother with Saethre-Chotzen syndrome demonstrated an apparently balanced translocation, t(2;7)(p23;p22). This association lends support to localization of the gene for Saethre-Chotzen syndrome to the 7p2 region and supports further involvement of gene(s) in the 7p22 region. (C) 1993 Wiley-Liss, Inc.
Document Type: Article
Language: English
Addresses:
1. UNIV MED & DENT NEW JERSEY, ROBERT WOOD JOHNSON MED SCH, DIV PEDIAT GENET, CAMDEN, NJ USA
2. UNIV MED & DENT NEW JERSEY, ROBERT WOOD JOHNSON MED SCH, DIV PEDIAT HEMATOL ONCOL, CAMDEN, NJ USA
3. UNIV PENN, CHILDRENS HOSP, SCH MED, DIV HUMAN GENET & MOLEC BIOL, PHILADELPHIA, PA 19104 USA
4. DALHOUSIE UNIV, FAC DENT, HALIFAX B3H 4H2, NS CANADA
5. DALHOUSIE UNIV, DEPT MED, HALIFAX B3H 4H2, NS CANADA
6. JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA
Publisher: WILEY-LISS, DIV JOHN WILEY & SONS INC 605 THIRD AVE, NEW YORK, NY 10158-0012
Subject Category: Genetics & Heredity
IDS Number: MA176
ISSN: 0148-7299
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