142 related articles for article (PubMed ID: 2889663)
1. Prenatal diagnosis of X-linked chronic granulomatous disease using restriction fragment length polymorphism analysis.
Lindlöf M; Kere J; Ristola M; Repo H; Leirisalo-Repo M; von Koskull H; Ammälä P; de la Chapelle A
Genomics; 1987 Sep; 1(1):87-92. PubMed ID: 2889663
[TBL] [Abstract][Full Text] [Related]
2. Identification of (CA/GT)n polymorphisms within the X-linked chronic granulomatous disease (X-CGD) gene: utility for prenatal diagnosis.
Gorlin JB
J Pediatr Hematol Oncol; 1998; 20(2):112-9. PubMed ID: 9544160
[TBL] [Abstract][Full Text] [Related]
3. RFLP and deletion analysis for X-linked chronic granulomatous disease using the cDNA probe: potential for improved prenatal diagnosis and carrier determination.
Pelham A; O'Reilly MA; Malcolm S; Levinsky RJ; Kinnon C
Blood; 1990 Aug; 76(4):820-4. PubMed ID: 1974472
[TBL] [Abstract][Full Text] [Related]
4. Origin of mutations in two families with X-linked chronic granulomatous disease.
Francke U; Ochs HD; Darras BT; Swaroop A
Blood; 1990 Aug; 76(3):602-6. PubMed ID: 1974155
[TBL] [Abstract][Full Text] [Related]
5. Characterization of the p67phox gene: genomic organization and restriction fragment length polymorphism analysis for prenatal diagnosis in chronic granulomatous disease.
Kenney RT; Malech HL; Epstein ND; Roberts RL; Leto TL
Blood; 1993 Dec; 82(12):3739-44. PubMed ID: 7903171
[TBL] [Abstract][Full Text] [Related]
6. Nitroblue tetrazolium slide test. Use of the phorbol-myristate-acetate-stimulated NBT-reduction slide test for routine and prenatal detection of chronic granulomatous disease and diagnosis of heterozygous carriers.
Johansen KS
Acta Pathol Microbiol Immunol Scand C; 1983 Dec; 91(6):349-54. PubMed ID: 6673503
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of chronic granulomatous disease.
Matthay KK; Golbus MS; Wara DW; Mentzer WC
Am J Med Genet; 1984 Apr; 17(4):731-9. PubMed ID: 6720741
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of chronic granulomatous disease (CGD) in four high risk male fetuses.
Huu TP; Dumez Y; Marquetty C; Durandy A; Boue J; Hakim J
Prenat Diagn; 1987 May; 7(4):253-60. PubMed ID: 3588543
[TBL] [Abstract][Full Text] [Related]
9. A fast and easy nitroblue tetrazolium method for carrier screening and prenatal detection of chronic granulomatous disease.
Ayatollahi M; Tabei Z; Ramzi M; Kashef S; Haghshenas M
Arch Iran Med; 2006 Oct; 9(4):335-8. PubMed ID: 17061605
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis in a family with X-linked chronic granulomatous disease with the use of the polymerase chain reaction.
De Boer M; Bolscher BG; Sijmons RH; Scheffer H; Weening RS; Roos D
Prenat Diagn; 1992 Sep; 12(9):773-7. PubMed ID: 1438069
[TBL] [Abstract][Full Text] [Related]
11. Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms.
Moodie P; Liddell MB; Peake IR; Bloom AL
Br J Haematol; 1988 Sep; 70(1):77-84. PubMed ID: 2902876
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of chronic granulomatous disease in a male fetus.
Yavuz Köker M; Metin A; Ozgür TT; de Boer M; Roos D
Iran J Allergy Asthma Immunol; 2009 Mar; 8(1):57-61. PubMed ID: 19279361
[TBL] [Abstract][Full Text] [Related]
13. DNA linkage analysis of X chromosome-linked chronic granulomatous disease.
Baehner RL; Kunkel LM; Monaco AP; Haines JL; Conneally PM; Palmer C; Heerema N; Orkin SH
Proc Natl Acad Sci U S A; 1986 May; 83(10):3398-401. PubMed ID: 3010296
[TBL] [Abstract][Full Text] [Related]
14. X chromosome linked immunodeficiency.
Schwaber J; Rosen FS
Immunodefic Rev; 1990; 2(3):233-51. PubMed ID: 1981831
[TBL] [Abstract][Full Text] [Related]
15. [Prenatal diagnosis of chronic granulomatous disease by percutaneous umbilical blood sampling].
Murotsuki J; Uehara S; Okamura K; Yajima A
Nihon Sanka Fujinka Gakkai Zasshi; 1993 Nov; 45(11):1353-5. PubMed ID: 8258738
[No Abstract] [Full Text] [Related]
16. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
Lindlöf M; Kääriäinen H; Davies KE; de la Chapelle A
J Med Genet; 1986 Dec; 23(6):560-72. PubMed ID: 2879928
[TBL] [Abstract][Full Text] [Related]
17. [Exclusion prenatal diagnosis of chronic familial septic granulomatosis].
Pham Huu T; Dumez Y; Durand A; Le Merrer M; Lemerle-Gruson S; Hakim J; Griscelli C
Arch Fr Pediatr; 1985 Feb; 42(2):103-5. PubMed ID: 4004464
[TBL] [Abstract][Full Text] [Related]
18. An additional NsiI RFLP at the X-linked chronic granulomatous disease (CYBB) locus.
Pelham A; Malcolm S; Levinsky RJ; Kinnon C
Nucleic Acids Res; 1990 Dec; 18(23):7199. PubMed ID: 1979867
[No Abstract] [Full Text] [Related]
19. Carrier screening and prenatal detection of chronic granulomatous disease in Iran.
Ayatollahi M; Geramizadeh B
Saudi Med J; 2006 Sep; 27(9):1334-7. PubMed ID: 16951769
[TBL] [Abstract][Full Text] [Related]
20. RFLPs tightly linked with cystic fibrosis: value of probes at the D7S23 locus in prenatal diagnosis.
Vasseur F; Flactif M; Savary JB; Turpin D; Deminatti MM
Ann Genet; 1989; 32(2):78-81. PubMed ID: 2569290
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]