[Partial monosomy of the short arm of chromosome 10, associated with Rieger's syndrome and a Di George type partial immunodeficiency] - PubMed (original) (raw)
[Article in French]
- PMID: 6712103
Case Reports
[Partial monosomy of the short arm of chromosome 10, associated with Rieger's syndrome and a Di George type partial immunodeficiency]
[Article in French]
J Hervé et al. Ann Pediatr (Paris). 1984 Jan.
No abstract available
Similar articles
- Di George anomaly associated with a de novo Y;22 translocation resulting in monosomy del(22)(q11.2).
Lupski JR, Langston C, Friedman R, Ledbetter DH, Greenberg F. Lupski JR, et al. Am J Med Genet. 1991 Aug 1;40(2):196-8. doi: 10.1002/ajmg.1320400214. Am J Med Genet. 1991. PMID: 1897574 - [Prenatal diagnosis of te Dandy-Walker syndrome associated with partial trisomy of chromosome 9].
Zacharias S, Nazer J, Lacassie I, Ibarra A, Valencia JM. Zacharias S, et al. Rev Chil Obstet Ginecol. 1983;48(6):414-8. Rev Chil Obstet Ginecol. 1983. PMID: 6681216 Spanish. No abstract available. - [Monosomy 22pter-22q11.2 with monosomy 10q26.2-10qter without Di George syndrome].
Arslanian A, Veneziano G, Grasso M, Brugo A, Bertamino F. Arslanian A, et al. Pathologica. 1985 Nov-Dec;77(1052):767-70. Pathologica. 1985. PMID: 3842998 Italian. No abstract available. - Partial monosomy 22 as result of an X/22 translocation in a newborn with DiGeorge syndrome.
Schwanitz G, Zerres K. Schwanitz G, et al. Ann Genet. 1987;30(2):80-4. Ann Genet. 1987. PMID: 3314667 Review. - DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.
Demczuk S, Aurias A. Demczuk S, et al. Ann Genet. 1995;38(2):59-76. Ann Genet. 1995. PMID: 7486827 Review.
Cited by
- Chromosome abnormalities and the genetics of congenital corneal opacification.
Mataftsi A, Islam L, Kelberman D, Sowden JC, Nischal KK. Mataftsi A, et al. Mol Vis. 2011;17:1624-40. Epub 2011 Jun 17. Mol Vis. 2011. PMID: 21738392 Free PMC article. Review. - An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.
Frank DU, Fotheringham LK, Brewer JA, Muglia LJ, Tristani-Firouzi M, Capecchi MR, Moon AM. Frank DU, et al. Development. 2002 Oct;129(19):4591-603. doi: 10.1242/dev.129.19.4591. Development. 2002. PMID: 12223415 Free PMC article. - A second locus for Rieger syndrome maps to chromosome 13q14.
Phillips JC, del Bono EA, Haines JL, Pralea AM, Cohen JS, Greff LJ, Wiggs JL. Phillips JC, et al. Am J Hum Genet. 1996 Sep;59(3):613-9. Am J Hum Genet. 1996. PMID: 8751862 Free PMC article. - Human chromosome 22.
Kaplan JC, Aurias A, Julier C, Prieur M, Szajnert MF. Kaplan JC, et al. J Med Genet. 1987 Feb;24(2):65-78. doi: 10.1136/jmg.24.2.65. J Med Genet. 1987. PMID: 3550088 Free PMC article. Review. - Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.
Greenberg F, Elder FF, Haffner P, Northrup H, Ledbetter DH. Greenberg F, et al. Am J Hum Genet. 1988 Nov;43(5):605-11. Am J Hum Genet. 1988. PMID: 3189331 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Molecular Biology Databases