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An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA

Document Type

Article

Author

Lalande, M.; Trask, B.J.; Massa, H.; Overhauser, J.; Lansdorp, P.M.; Katz, S.G.; Schneider, S.S.; Bartuski, A.; Silverman, G.A.

Source

In: Human Molecular Genetics. (Human Molecular Genetics, 1999, 8(1):87-92)

Subject

Language

English

ISSN

09646906

Online Access

Full Text (Oxford University Press) Full Text (OUP Near Archive) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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