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5. Nijmegen breakage syndrome in 13% of age-matched Czech children with primary microcephaly. Seeman P; Gebertová K; Paderová K; Sperling K; Seemanová E Pediatr Neurol; 2004 Mar; 30(3):195-200. PubMed ID: 15033202 [TBL] [Abstract][Full Text] [Related]
6. Severe microcephaly with normal intellectual development: the Nijmegen breakage syndrome. Green AJ; Yates JR; Taylor AM; Biggs P; McGuire GM; McConville CM; Billing CJ; Barnes ND Arch Dis Child; 1995 Nov; 73(5):431-4. PubMed ID: 8554361 [TBL] [Abstract][Full Text] [Related]
7. A new chromosomal instability disorder confirmed by complementation studies. Wegner RD; Metzger M; Hanefeld F; Jaspers NG; Baan C; Magdorf K; Kunze J; Sperling K Clin Genet; 1988 Jan; 33(1):20-32. PubMed ID: 3277755 [TBL] [Abstract][Full Text] [Related]
8. Variants of Nijmegen breakage syndrome and ataxia telangiectasia. Weemaes CM; Smeets DF; Horstink M; Haraldsson A; Bakkeren JA Immunodeficiency; 1993; 4(1-4):109-11. PubMed ID: 7513225 [TBL] [Abstract][Full Text] [Related]
9. Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndrome. Di Rocco M; Arslanian A; Romanengo M; Dagna-Bricarelli F; Borrone C J Med Genet; 1999 Feb; 36(2):159-60. PubMed ID: 10051019 [TBL] [Abstract][Full Text] [Related]
10. Chromosome instability with bleomycin and X-ray hypersensitivity in a boy with Nijmegen breakage syndrome. Pérez-Vera P; González-del Angel A; Molina B; Gómez L; Frías S; Gatti RA; Carnevale A Am J Med Genet; 1997 May; 70(1):24-7. PubMed ID: 9129736 [TBL] [Abstract][Full Text] [Related]
11. [Down syndrome: pathogenesis, radioresistant DNA synthesis and chromosomal instability]. Barenfel'd LS Tsitologiia; 2002; 44(4):379-86. PubMed ID: 12149783 [TBL] [Abstract][Full Text] [Related]
12. Possible new variant of Nijmegen breakage syndrome. Der Kaloustian VM; Kleijer W; Booth A; Auerbach AD; Mazer B; Elliott AM; Abish S; Usher R; Watters G; Vekemans M; Eydoux P Am J Med Genet; 1996 Oct; 65(1):21-6. PubMed ID: 8914736 [TBL] [Abstract][Full Text] [Related]
14. Positional cloning of the gene for Nijmegen breakage syndrome. Matsuura S; Tauchi H; Nakamura A; Kondo N; Sakamoto S; Endo S; Smeets D; Solder B; Belohradsky BH; Der Kaloustian VM; Oshimura M; Isomura M; Nakamura Y; Komatsu K Nat Genet; 1998 Jun; 19(2):179-81. PubMed ID: 9620777 [TBL] [Abstract][Full Text] [Related]
15. ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome. Curry CJ; O'Lague P; Tsai J; Hutchison HT; Jaspers NG; Wara D; Gatti RA Am J Hum Genet; 1989 Aug; 45(2):270-5. PubMed ID: 2491181 [TBL] [Abstract][Full Text] [Related]
16. Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies. Elejalde BR; Opitz JM; de Elejalde MM; Gilbert EF; Abellera M; Meisner L; Lebel RR; Hartigan JM Am J Med Genet; 1984 Apr; 17(4):723-30. PubMed ID: 6539070 [TBL] [Abstract][Full Text] [Related]
17. Characterization of cell cycle checkpoint responses after ionizing radiation in Nijmegen breakage syndrome cells. Yamazaki V; Wegner RD; Kirchgessner CU Cancer Res; 1998 Jun; 58(11):2316-22. PubMed ID: 9622065 [TBL] [Abstract][Full Text] [Related]