72 related articles for article (PubMed ID: 2879657)
1. Marfan syndrome: exclusion of genetic linkage to the COL1A2 gene.
Tsipouras P; Børresen AL; Bamforth S; Harper PS; Berg K
Clin Genet; 1986 Nov; 30(5):428-32. PubMed ID: 2879657
[TBL] [Abstract][Full Text] [Related]
2. Marfan syndrome: exclusion of genetic linkage to three major collagen genes.
Francomano CA; Streeten EA; Meyers DA; Pyeritz RE
Am J Med Genet; 1988 Feb; 29(2):457-62. PubMed ID: 3354620
[TBL] [Abstract][Full Text] [Related]
3. Exclusion of the alpha 2(I) and alpha 1(III) collagen genes as the mutant loci in a Marfan syndrome family.
Dalgleish R; Hawkins JR; Keston M
J Med Genet; 1987 Mar; 24(3):148-51. PubMed ID: 2883320
[TBL] [Abstract][Full Text] [Related]
4. Heterozygous TGFBR2 mutations in Marfan syndrome.
Mizuguchi T; Collod-Beroud G; Akiyama T; Abifadel M; Harada N; Morisaki T; Allard D; Varret M; Claustres M; Morisaki H; Ihara M; Kinoshita A; Yoshiura K; Junien C; Kajii T; Jondeau G; Ohta T; Kishino T; Furukawa Y; Nakamura Y; Niikawa N; Boileau C; Matsumoto N
Nat Genet; 2004 Aug; 36(8):855-60. PubMed ID: 15235604
[TBL] [Abstract][Full Text] [Related]
5. Linkage analysis of five fibrillar collagen loci in a large French Marfan syndrome family.
Boileau C; Jondeau G; Bonaiti C; Coulon M; Delorme G; Dubourg O; Bourdarias JP; Junien C
J Med Genet; 1990 Feb; 27(2):78-81. PubMed ID: 1969488
[TBL] [Abstract][Full Text] [Related]
6. Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families.
Mottes M; Sangalli A; Pignatti PF
Am J Med Genet; 1993 Jan; 45(2):217-22. PubMed ID: 8096115
[TBL] [Abstract][Full Text] [Related]
7. Haplotype analysis enables the diagnosis of Marfan syndrome.
Basel D; Kilpatrick MW; Tsipouras P
Conn Med; 2004; 68(6):363-6. PubMed ID: 15266886
[TBL] [Abstract][Full Text] [Related]
8. Amplified fragment length polymorphism analysis on D5S436 locus and its application to linkage analysis in gene diagnosis of asthma.
Huang K; Weng X; Liu J; Zhu Z; Xiao B; Yan M; Zhang H; Wang C
Chin Med J (Engl); 1999 Feb; 112(2):112-4. PubMed ID: 11593573
[TBL] [Abstract][Full Text] [Related]
9. Genetic analysis of structural elastic fiber and collagen genes in familial adolescent idiopathic scoliosis.
Miller NH; Mims B; Child A; Milewicz DM; Sponseller P; Blanton SH
J Orthop Res; 1996 Nov; 14(6):994-9. PubMed ID: 8982144
[TBL] [Abstract][Full Text] [Related]
10. Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia.
Burns TM; Te Morsche RH; Jansen JB; Drenth JP
Br J Dermatol; 2005 Jul; 153(1):174-7. PubMed ID: 16029345
[TBL] [Abstract][Full Text] [Related]
11. Carrier detection in severe (type III) von Willebrand disease using two intragenic restriction fragment length polymorphisms.
Bahnak BR; Lavergne JM; Verweij CL; Rothschild C; Pannekoek H; Larrieu MJ; Meyer D
Thromb Haemost; 1988 Oct; 60(2):178-81. PubMed ID: 2905841
[TBL] [Abstract][Full Text] [Related]
12. Segregation of all four major fibrillar collagen genes in the Marfan syndrome.
Ogilvie DJ; Wordsworth BP; Priestley LM; Dalgleish R; Schmidtke J; Zoll B; Sykes BC
Am J Hum Genet; 1987 Dec; 41(6):1071-82. PubMed ID: 3479900
[TBL] [Abstract][Full Text] [Related]
13. Linkage analysis in Marfan syndrome.
Schwartz RC; Blanton SH; Hyde CA; Sottile TR; Hudgins L; Sarfarazi M; Tsipouras P
J Med Genet; 1990 Feb; 27(2):86-90. PubMed ID: 1969490
[TBL] [Abstract][Full Text] [Related]
14. Correlation of linkage data with phenotype in eight families with Stickler syndrome.
Wilkin DJ; Mortier GR; Johnson CL; Jones MC; de Paepe A; Shohat M; Wildin RS; Falk RE; Cohn DH
Am J Med Genet; 1998 Nov; 80(2):121-7. PubMed ID: 9805127
[TBL] [Abstract][Full Text] [Related]
15. Genetic linkage of two intragenic restriction fragment length polymorphisms with von Willebrand's disease type IIA. Evidence for a defect in the von Willebrand factor gene.
Verweij CL; Quadt R; Briët E; Dubbeldam K; van Ommen GB; Pannekoek H
J Clin Invest; 1988 Apr; 81(4):1116-21. PubMed ID: 2895123
[TBL] [Abstract][Full Text] [Related]
16. TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome.
Singh KK; Rommel K; Mishra A; Karck M; Haverich A; Schmidtke J; Arslan-Kirchner M
Hum Mutat; 2006 Aug; 27(8):770-7. PubMed ID: 16799921
[TBL] [Abstract][Full Text] [Related]
17. A highly polymorphic (ACT)n VNTR (variable nucleotide of tandem repeats) locus inside intron 12 of COL1A2, one of the two genes involved in dominant osteogenesis imperfecta.
Pepe G
Hum Mutat; 1993; 2(4):300-5. PubMed ID: 8104634
[TBL] [Abstract][Full Text] [Related]
18. Linkage data for Marfan syndrome and markers on chromosomes 1 and 11.
de Groote J; Farndon PA; Kilpatrick MV; de Paepe A; Oorthuys JW; Nevin NC; Child AH; Pope FM
J Med Genet; 1990 Feb; 27(2):82-5. PubMed ID: 1969489
[TBL] [Abstract][Full Text] [Related]
19. Marfan syndrome: exclusion of genetic linkage to five genes coding for connective tissue components in the long arm of chromosome 2.
Kainulainen K; Savolainen A; Palotie A; Kaitila I; Rosenbloom J; Peltonen L
Hum Genet; 1990 Feb; 84(3):233-6. PubMed ID: 1968032
[TBL] [Abstract][Full Text] [Related]
20. [The Ehlers-Danlos and Marfan syndromes in young children].
De Paepe A; Van den Bossche H; Mortier G; Matton M
J Genet Hum; 1988 Jun; 36(3):247-53. PubMed ID: 3411305
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]