Interstitial deletion of the short arm of chromosome 10: Report of a case and review of the literature

Author:

Kato Zenichiro,Kato Tomomi,Kondo Naomi,Orii Tadao

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical)

Reference14 articles.

1. Danesino C, Lo Curto F, Bonfant G, Cazzadore C, Voltolin G, Bersi S (1984): Deficiency 10p. Report of a case and exclusion mapping of the hexokinase 1 locus to band 10p11.2. Ann Génét27: 162–166

2. Elliot D, Thomas GH, Condon CJ, Khuri N, Richardson F (1970): C-group chromosome abnormality (?10p−). Am. J Dis Child110: 72–73

3. Elstner CL, Carey JC, Livingston G, Moeschler J, Lubinsky M (1984): Further delineation of the 10p deletion syndrome. Pediatrics73: 670–675

4. Genick A, Brönniman U, Tobler R, auf der Maur P (1983): Partial monosomy of chromosome 10 short arms. J Med Genet20: 107–111

5. Greenberg F, Valdes C, Rosenblatt HM, Kirkland JL, Ledbetter DH (1986): Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome. J Pediatr109: 489–492

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