Skip to main content

letter

. 1997 Dec;61(6):1456–1459. doi: 10.1086/301652

Goosecoid-like sequences and the smallest region of deletion overlap in DiGeorge and velocardiofacial syndromes.

A Pragliola, V Jurecic, C K Chau, N Philip, A Baldini

PMCID: PMC1716100 PMID: 9399910

1456

Images in this article

Figure 1
on p.1457

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Dallapiccola B., Pizzuti A., Novelli G. How many breaks do we need to CATCH on 22q11? Am J Hum Genet. 1996 Jul;59(1):7–11. [PMC free article] [PubMed] [Google Scholar]
Galili N., Baldwin H. S., Lund J., Reeves R., Gong W., Wang Z., Roe B. A., Emanuel B. S., Nayak S., Mickanin C. A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region. Genome Res. 1997 Jan;7(1):17–26. doi: 10.1101/gr.7.1.17. [DOI] [PubMed] [Google Scholar]
Gong W., Emanuel B. S., Collins J., Kim D. H., Wang Z., Chen F., Zhang G., Roe B., Budarf M. L. A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11. Hum Mol Genet. 1996 Jun;5(6):789–800. doi: 10.1093/hmg/5.6.789. [DOI] [PubMed] [Google Scholar]
Gottlieb S., Emanuel B. S., Driscoll D. A., Sellinger B., Wang Z., Roe B., Budarf M. L. The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development. Am J Hum Genet. 1997 May;60(5):1194–1201. [PMC free article] [PubMed] [Google Scholar]
Kurahashi H., Nakayama T., Osugi Y., Tsuda E., Masuno M., Imaizumi K., Kamiya T., Sano T., Okada S., Nishisho I. Deletion mapping of 22q11 in CATCH22 syndrome: identification of a second critical region. Am J Hum Genet. 1996 Jun;58(6):1377–1381. [PMC free article] [PubMed] [Google Scholar]
Levy A., Demczuk S., Aurias A., Depétris D., Mattei M. G., Philip N. Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome. Hum Mol Genet. 1995 Dec;4(12):2417–2419. doi: 10.1093/hmg/4.12.2417. [DOI] [PubMed] [Google Scholar]
Lindsay E. A., Halford S., Wadey R., Scambler P. J., Baldini A. Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization. Genomics. 1993 Aug;17(2):403–407. doi: 10.1006/geno.1993.1339. [DOI] [PubMed] [Google Scholar]
Lindsay E. A., Rizzu P., Antonacci R., Jurecic V., Delmas-Mata J., Lee C. C., Kim U. J., Scambler P. J., Baldini A. A transcription map in the CATCH22 critical region: identification, mapping, and ordering of four novel transcripts expressed in heart. Genomics. 1996 Feb 15;32(1):104–112. doi: 10.1006/geno.1996.0082. [DOI] [PubMed] [Google Scholar]

ACTIONS

RESOURCES