Chromosomal deletion 4p15.32→p14 in a treacher collins syndrome patient: Exclusion of the disease locus from and mapping of anonymous DNA sequences to this region-Reference-Cited by-同舟云学术

Chromosomal deletion 4p15.32→p14 in a treacher collins syndrome patient: Exclusion of the disease locus from and mapping of anonymous DNA sequences to this region

Published:1991-09 Issue:1 Volume:11 Page:188-192
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

Jabs Ethylin Wang,Coss Cathleen A.,Hayflick Susan J.,Whitmore Theodore E.,Pauli Richard M.,Kirkpatrick Susan J.,Meyers Deborah A.,Goldberg Rosalie,Day Donald W.,Rosenbaum Kenneth N.

Publisher

Elsevier BV

Subject

Genetics

Reference23 articles.

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2. Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase;Balestrazzi;Hum. Genet,1983

3. Clinical Atlas of Human Chromosomes,1984

4. Association of Treacher Collins syndrome and translocation 6p21.3116p13.11: Exclusion of the locus from these candidate regions;Dixon;Am. J. Hum. Genet,1991

5. Mandibulo-facial dysostosis;Fazen;Am. J. Dis. Child,1967

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