Tsipouras P - Search Results

1

Exclusion of COL2A1 as a candidate gene in a family with Wagner-Stickler syndrome.

Fryer AE, Upadhyaya M, Littler M, Bacon P, Watkins D, Tsipouras P, Harper PS. Fryer AE, et al. Among authors: tsipouras p. J Med Genet. 1990 Feb;27(2):91-3. doi: 10.1136/jmg.27.2.91. J Med Genet. 1990. PMID: 2319589 Free PMC article.

2

Marfan syndrome: exclusion of genetic linkage to the COL1A2 gene.

Tsipouras P, Børresen AL, Bamforth S, Harper PS, Berg K. Tsipouras P, et al. Clin Genet. 1986 Nov;30(5):428-32. Clin Genet. 1986. PMID: 2879657

3

Mild spondyloepiphyseal dysplasia (Namaqualand type): genetic linkage to the type II collagen gene COL2A1.

Sher C, Ramesar R, Martell R, Learmonth I, Tsipouras P, Beighton P. Sher C, et al. Among authors: tsipouras p. Am J Hum Genet. 1991 Mar;48(3):518-24. Am J Hum Genet. 1991. PMID: 1671807 Free PMC article.

4

Prenatal prediction of osteogenesis imperfecta (OI type IV): exclusion of inheritance using a collagen gene probe.

Tsipouras P, Schwartz RC, Goldberg JD, Berkowitz RL, Ramirez F. Tsipouras P, et al. J Med Genet. 1987 Jul;24(7):406-9. doi: 10.1136/jmg.24.7.406. J Med Genet. 1987. PMID: 2886666 Free PMC article.

5

A split hand-split foot (SHFM3) gene is located at 10q24-->25.

Gurrieri F, Prinos P, Tackels D, Kilpatrick MW, Allanson J, Genuardi M, Vuckov A, Nanni L, Sangiorgi E, Garofalo G, Nunes ME, Neri G, Schwartz C, Tsipouras P. Gurrieri F, et al. Among authors: tsipouras p. Am J Med Genet. 1996 Apr 24;62(4):427-36. doi: 10.1002/(SICI)1096-8628(19960424)62:4<427::AID-AJMG16>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8723077

6

Molecular nosology of heritable disorders of connective tissue.

Beighton P, De Paepe A, Hall JG, Hollister DW, Pope FM, Pyeritz RE, Steinmann B, Tsipouras P. Beighton P, et al. Among authors: tsipouras p. Am J Med Genet. 1992 Feb 15;42(4):431-48. doi: 10.1002/ajmg.1320420406. Am J Med Genet. 1992. PMID: 1609825 No abstract available.

7

Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagen.

Anderson IJ, Tsipouras P, Scher C, Ramesar RS, Martell RW, Beighton P. Anderson IJ, et al. Among authors: tsipouras p. Am J Med Genet. 1990 Oct;37(2):272-6. doi: 10.1002/ajmg.1320370223. Am J Med Genet. 1990. PMID: 1978986

8

The expanding panorama of split hand foot malformation.

Basel D, Kilpatrick MW, Tsipouras P. Basel D, et al. Among authors: tsipouras p. Am J Med Genet A. 2006 Jul 1;140(13):1359-65. doi: 10.1002/ajmg.a.31304. Am J Med Genet A. 2006. PMID: 16763964 Review.

9

Genetic disorders of collagen.

Tsipouras P, Ramirez F. Tsipouras P, et al. J Med Genet. 1987 Jan;24(1):2-8. doi: 10.1136/jmg.24.1.2. J Med Genet. 1987. PMID: 3543367 Free PMC article. Review.

10

Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK).

Beighton P, De Paepe A, Steinmann B, Tsipouras P, Wenstrup RJ. Beighton P, et al. Among authors: tsipouras p. Am J Med Genet. 1998 Apr 28;77(1):31-7. doi: 10.1002/(sici)1096-8628(19980428)77:1<31::aid-ajmg8>3.0.co;2-o. Am J Med Genet. 1998. PMID: 9557891

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