108 related articles for article (PubMed ID: 1887849)
1. Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded child.
Barbi G; Scheres JM; Schindler D; Taalman RD; Rodens K; Mehnert K; Müller M; Seyschab H
Am J Med Genet; 1991 Jul; 40(1):44-50. PubMed ID: 1887849
[TBL] [Abstract][Full Text] [Related]
2. Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndrome.
Chrzanowska KH; Kleijer WJ; Krajewska-Walasek M; Białecka M; Gutkowska A; Goryluk-Kozakiewicz B; Michałkiewicz J; Stachowski J; Gregorek H; Lysón-Wojciechowska G
Am J Med Genet; 1995 Jul; 57(3):462-71. PubMed ID: 7545870
[TBL] [Abstract][Full Text] [Related]
3. Further delineation of the Nijmegen breakage syndrome.
Taalman RD; Hustinx TW; Weemaes CM; Seemanová E; Schmidt A; Passarge E; Scheres JM
Am J Med Genet; 1989 Mar; 32(3):425-31. PubMed ID: 2786340
[TBL] [Abstract][Full Text] [Related]
4. [Microcephaly with chromosomal instability and immunodeficiency--Nijmegen syndrome].
Chrzanowska KH
Pediatr Pol; 1996 Mar; 71(3):223-34. PubMed ID: 8966094
[TBL] [Abstract][Full Text] [Related]
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]
13. [Clinico-genetic diagnosis of ataxia telangiectatica (Louis-Bar syndrome)].
Fuhrmann E; Pfeiffer L; Zschenderlein R; Leonhardt T; Melster U; Kölmel HW
Nervenarzt; 1993 Feb; 64(2):140-2. PubMed ID: 8450897
[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]
18. Chromosomal breakage syndromes.
Carney JP
Curr Opin Immunol; 1999 Aug; 11(4):443-7. PubMed ID: 10448147
[TBL] [Abstract][Full Text] [Related]
19. Combined immunodeficiency associated with increased apoptosis of lymphocytes and radiosensitivity fibroblasts.
Peake J; Waugh A; Le Deist F; Priestley A; Rieux-Laucat F; Foray N; Capulas E; Singleton BK; de Villartay JP; Cant A; Malaise EP; Fischer A; Hivroz C; Jeggo PA
Cancer Res; 1999 Jul; 59(14):3454-60. PubMed ID: 10416610
[TBL] [Abstract][Full Text] [Related]
20. [A new syndrome of mental retardation and chromosomic instability in 3 siblings].
Carnevale A; Molina B; Cardona M
Rev Invest Clin; 1989; 41(3):259-64. PubMed ID: 2814001
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
