125 related articles for article (PubMed ID: 7705830)
1. Mucopolysaccharidosis IVA: structural gene alterations identified by Southern blot analysis and identification of racial differences.
Tomatsu S; Fukuda S; Cooper A; Wraith JE; Uchiyama A; Hori T; Nakashima Y; Yamada N; Sukegawa K; Kondo N
Hum Genet; 1995 Apr; 95(4):376-81. PubMed ID: 7705830
[TBL] [Abstract][Full Text] [Related]
2. Mucopolysaccharidosis IVA: polymorphic haplotypes and informative RFLPs in the Japanese population.
Iwata H; Tomatsu S; Fukuda S; Uchiyama A; Rezvi GM; Ogawa T; Hori T; Nakashima Y; Yamagishi A; Sukegawa K
Hum Genet; 1995 Mar; 95(3):257-64. PubMed ID: 7532616
[TBL] [Abstract][Full Text] [Related]
3. Mucopolysaccharidosis type II (Hunter disease): 13 gene mutations in 52 Japanese patients and carrier detection in four families.
Yamada Y; Tomatsu S; Sukegawa K; Suzuki Y; Kondo N; Hopwood JJ; Orii T
Hum Genet; 1993 Sep; 92(2):110-4. PubMed ID: 8370574
[TBL] [Abstract][Full Text] [Related]
4. Mucopolysaccharidosis IVA: a comparative study of polymorphic DNA haplotypes in the Caucasian and Japanese populations.
Rezvi GM; Tomatsu S; Fukuda S; Yamagishi A; Cooper A; Wraith JE; Iwata H; Kato Z; Yamada N; Sukegawa K; Shimozawa N; Suzuki Y; Kondo N; Orii T
J Inherit Metab Dis; 1996; 19(3):301-8. PubMed ID: 8803772
[TBL] [Abstract][Full Text] [Related]
5. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
6. Structural gene aberrations in mucopolysaccharidosis II (Hunter).
Wehnert M; Hopwood JJ; Schröder W; Herrmann FH
Hum Genet; 1992 Jun; 89(4):430-2. PubMed ID: 1352274
[TBL] [Abstract][Full Text] [Related]
7. DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations.
Goto K; Lee JH; Matsuda C; Hirabayashi K; Kojo T; Nakamura A; Mitsunaga Y; Furukawa T; Sahashi K; Arahata K
Neuromuscul Disord; 1995 May; 5(3):201-8. PubMed ID: 7633185
[TBL] [Abstract][Full Text] [Related]
8. Associations between restriction fragment length polymorphisms detected with a probe for human C4 and allotype of C4B5 allele.
Kobayashi K; Atoh M; Hara M; Tanaka H; Itoh K; Hirakawa K; Sekiguchi S
Hum Immunol; 1990 Sep; 29(1):3-13. PubMed ID: 1976612
[TBL] [Abstract][Full Text] [Related]
9. The rabbit alpha-like globin gene cluster is polymorphic both in the sizes of BamHI fragments and in the numbers of duplicated sets of genes.
Cheng JF; Hardison RC
Mol Biol Evol; 1988 Sep; 5(5):486-98. PubMed ID: 2904112
[TBL] [Abstract][Full Text] [Related]
10. Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.
Donohoue PA; van Dop C; McLean RH; White PC; Jospe N; Migeon CJ
J Clin Endocrinol Metab; 1986 May; 62(5):995-1002. PubMed ID: 3007562
[TBL] [Abstract][Full Text] [Related]
11. Detection of immunoglobulin kappa light-chain gene rearrangement patterns by Southern blot analysis.
Beishuizen A; Verhoeven MA; Mol EJ; van Dongen JJ
Leukemia; 1994 Dec; 8(12):2228-36; discussion 2237-9. PubMed ID: 7808012
[TBL] [Abstract][Full Text] [Related]
12. Feline adult beta-globin polymorphism reflected in restriction fragment length patterns.
Kohn B; Henthorn PS; Rajpurohit Y; Reilly MP; Asakura T; Giger U
J Hered; 1999; 90(1):177-81. PubMed ID: 9987927
[TBL] [Abstract][Full Text] [Related]
13. Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.
Morel Y; André J; Uring-Lambert B; Hauptmann G; Bétuel H; Tossi M; Forest MG; David M; Bertrand J; Miller WL
J Clin Invest; 1989 Feb; 83(2):527-36. PubMed ID: 2913051
[TBL] [Abstract][Full Text] [Related]
14. Bam HI restriction fragment length polymorphisms for hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene of carriers and controls of HPRT deficiency in Japan.
Igarashi T; Ikegami H; Yamazaki H; Minami M
Acta Paediatr Jpn; 1990 Feb; 32(1):12-5. PubMed ID: 1970211
[TBL] [Abstract][Full Text] [Related]
15. Restriction fragment length polymorphism of bcr in Japanese patients with hematological malignancies.
Kato Y; Sawada H; Tashima M; Yumoto Y; Okuda T; Ueda T; Uchino H; Hotta T; Mitsutani S; Ono T
Leukemia; 1988 Oct; 2(10):701-3. PubMed ID: 2902258
[TBL] [Abstract][Full Text] [Related]
16. Heteroallelic missense mutations of the galactosamine-6-sulfate sulfatase (GALNS) gene in a mild form of Morquio disease (MPS IVA).
Cole DE; Fukuda S; Gordon BA; Rip JW; LeCouteur AN; Rupar CA; Tomatsu S; Ogawa T; Sukegawa K; Orii T
Am J Med Genet; 1996 Jun; 63(4):558-65. PubMed ID: 8826435
[TBL] [Abstract][Full Text] [Related]
17. Polymorphic class II sequences linked to the rat major histocompatibility complex (RT1) homologous to human DR and DQ sequences.
Palmer MJ; Buck DA; Frelinger JA; Wettstein PJ
J Immunol; 1985 Aug; 135(2):1450-5. PubMed ID: 2989367
[TBL] [Abstract][Full Text] [Related]
18. Restrictive fragment length polymorphisms of markers 3'HVR and 24-1 and their applications in gene diagnosis of adult polycystic disease in Chinese.
Zhang SZ; Ding L; Yu YL; Hu Y; Luo NF; Zhang SX; Li H
Chin Med J (Engl); 1994 Jan; 107(1):47-52. PubMed ID: 7910547
[TBL] [Abstract][Full Text] [Related]
19. Association between EcoRI fragment-length polymorphism of the immunoglobulin lambda variable 8 (IGLV8) gene family with rheumatoid arthritis and systemic lupus erythematosus.
Queiroz RG; Tamia-Ferreira MC; Carvalho IF; Petean FC; Passos GA
Braz J Med Biol Res; 2001 Apr; 34(4):525-8. PubMed ID: 11285465
[TBL] [Abstract][Full Text] [Related]
20. Two mutant alleles of the human cytochrome P-450db1 gene (P450C2D1) associated with genetically deficient metabolism of debrisoquine and other drugs.
Skoda RC; Gonzalez FJ; Demierre A; Meyer UA
Proc Natl Acad Sci U S A; 1988 Jul; 85(14):5240-3. PubMed ID: 2899325
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
