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CFC syndrome
Neri G, et al. Am J Med Genet A 2003. Among authors: Zollino M. PMID 12522802
Cryptic t(1;12)(q44;p13.3) translocation in a previously described syndrome with polymicrogyria, segregating as an apparently X-linked trait
Zollino M, et al. Am J Med Genet A 2003. PMID 12548742
We had previously reported it as an X-linked condition affecting four members (three males and one female) of a family [Zollino et al., 1992: Am J Med Genet 43:452-457]. ...
We had previously reported it as an X-linked condition affecting four members (three males and one female) of a family [Zollino et al …
The new Wolf-Hirschhorn syndrome critical region (WHSCR-2): a description of a second case
Rodríguez L, et al. Am J Med Genet A 2005. Among authors: Zollino M. PMID 15948183
This patient supports the recent proposal by Zollino et al. [2003] that the critical region for WHS is located distally to the WHSCR between the loci D4S3327 and D4S98-D4S16, and it is called "WHSCR-2" [Zollino et al., 2003]....
This patient supports the recent proposal by Zollino et al. [2003] that the critical region for WHS is located distally to the WHSCR …
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