Portal de Periódicos da CAPES

FAMILIAL APLASTIC ANAEMIA WITHOUT CONGENITAL MALFORMATIONS

1969; Wiley; Volume: 58; Issue: 2 Linguagem: Inglês

10.1111/j.1651-2227.1969.tb04699.x

1651-2227

Rina Zaizov, Y Matoth, Zipora Mamon,

Oral and Craniofacial Lesions

Acta PaediatricaVolume 58, Issue 2 p. 151-156 FAMILIAL APLASTIC ANAEMIA WITHOUT CONGENITAL MALFORMATIONS R. ZAIZOV, R. ZAIZOV Department of Paediatrics and Cytogenetic Laboratory, Beilinson Hospital, Petah Tikva, and Tel Aviv University Medical School, Israel (R. Z.) Department of Pediatrics, Beilinson Hospital, Petah-Tikva IsraelSearch for more papers by this authorY. MATOTH, Y. MATOTH Department of Paediatrics and Cytogenetic Laboratory, Beilinson Hospital, Petah Tikva, and Tel Aviv University Medical School, IsraelSearch for more papers by this authorZ. MAMON, Z. MAMON Department of Paediatrics and Cytogenetic Laboratory, Beilinson Hospital, Petah Tikva, and Tel Aviv University Medical School, IsraelSearch for more papers by this author R. ZAIZOV, R. ZAIZOV Department of Paediatrics and Cytogenetic Laboratory, Beilinson Hospital, Petah Tikva, and Tel Aviv University Medical School, Israel (R. Z.) Department of Pediatrics, Beilinson Hospital, Petah-Tikva IsraelSearch for more papers by this authorY. MATOTH, Y. MATOTH Department of Paediatrics and Cytogenetic Laboratory, Beilinson Hospital, Petah Tikva, and Tel Aviv University Medical School, IsraelSearch for more papers by this authorZ. MAMON, Z. MAMON Department of Paediatrics and Cytogenetic Laboratory, Beilinson Hospital, Petah Tikva, and Tel Aviv University Medical School, IsraelSearch for more papers by this author First published: March 1969 https://doi.org/10.1111/j.1651-2227.1969.tb04699.xCitations: 19AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Bloom, G. E., Wasner, S., Gerald, P. S. & Diamond, L. K.: Chromosome abnormalities in constitutional aplastic anaemia. New Eng J Med, 273: 8, 1966. 2 Buckton, K. E., Jacobs, P. A., Court Brown, W. M. & Doll, R.: A study of the chromosome damage persisting after X-ray therapy for ankylosing spondylitis. Lancet, II: 676, 1962. 3 Estren, S. & Dameshek, W.: Familial hypoplastic anemia of childhood. Report of eight cases in two families with beneficial effect of splenectomy in one case. Amer J Dis Child, 73: 671, 1947. 4 Fanconi, G.: Familiäre infantile perniziosaartige Anämie. (Perniziöses Blutbild und Konstitution.) Jahrb Kinderheilk, 117: 257, 1927. 5 Fanconi, G.: Familiäl constitutional panmyelocytopathy, Fanconi's anemia. I. Clinical aspects. Seminars in Hematology, 4: 233, 1967. 6 German, S., Archibald, R. & Bloom, D.: Chromosomal breakage in a rare and probably genetically determined syndrome of man. Science, 148: 506, 1965. 7 Nilsson, L. R.: Chronic pancytopenia with multiple congenital abnormalities (Fanconi's Anaemia). Acta Paediat Scand, 49: 518, 1960. 8 Rohr, K.: Familial panmyelophthisis. Blood, 4: 130, 1949. 9 Shahidi, N. T., Gerald, P. S. & Diamond, L. K.: Alkali-resistant hemoglobin in aplastic anemia of both acquired and congenital types. New Eng J Med, 266: 117, 1962. 10 Schmid, W., Schaerer, K., Baumann, T. H. & Fanconi, G.: Chromosomenbrüchigkeit bei der familiären Pannmyelopathie (Typus Fanconi). Schweiz Med Wschr, 95: 1461, 1965. 11 Schmid, W.: Familial constitutional panmyelocytopathy, Fanconi's anemia. II. A discussion of the cytogenetic findings in Fanconi's anemia. Seminars in Hematology, 4: 241, 1967. 12 Schroeder, T. M., Anschuetz, F. & Knopp, A.: Spontane Chromosomen-aberration bei familiärer Panmyelopathie. Human Genetik, 1: 194, 1964. 13 Swift, M. R. & Hirschhorn, K.: Fanconi's anemia. Inherited susceptibility to chromosome breakage in various tissues. Ann Internal Med, 65: 496, 1966. Citing Literature Volume58, Issue2March 1969Pages 151-156 ReferencesRelatedInformation