Deletion 14q(q24.3 to q32.1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of (?1-antitrypsin)-Reference-Cited by-同舟云学术

Deletion 14q(q24.3 to q32.1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of (?1-antitrypsin)

Published:1986-10 Issue:2 Volume:74 Page:190-192
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Yamamoto Y.,Sawa R.,Okamoto N.,Matsui A.,Yanagisawa M.,Ikemoto S.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00282092.pdf

Reference13 articles.

1. Camargo M, Cervenka J (1982) Patterns of DNA replication of human chromosomes. II. Replication map and replication model. Am J Hum Genet 34: 757?780

2. Chamberlin J, Magenis RE (1980) Parental origin of de novo chromosome rearrangements. Hum Genet 53: 343?347

3. Couturier J, Morichon-Delvallez N, Dutrillaux B (1985) Deletion of band 13q21 is compatible with normal phenotype. Hum Genet 70: 87?91

4. Cox DW, Markovic VD, Teshima IE (1982) Genes for immunoglobulin heavy chains and for ?1-antitrypsin are localized to specific regions of chromosome 14q. Nature 297: 428?430

5. Hirabayashi Y, Futamatagawa O, Kubono K, Kawajiri K (1986) An automated turbidimetric immunoassay for transferrin, haptoglobin, ?1-antitrypsin. Jpn J Clin Lab Automation (in press)

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