Castedo S - Search Results

1

Terminal deletion of Xp22.3 associated with contiguous gene syndrome: Léri-Weill dyschondrosteosis, developmental delay, and ichthyosis.

Vassal H, Medeira A, Cordeiro I, Santos HG, Castedo S, Saraiva C, da Silva PM, Monteiro C. Vassal H, et al. Among authors: castedo s. Am J Med Genet. 2001 Apr 1;99(4):331-4. doi: 10.1002/1096-8628(20010401)99:4<331::aid-ajmg1175>3.0.co;2-w. Am J Med Genet. 2001. PMID: 11252003 No abstract available.

2

Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype.

Tan-Sindhunata G, Castedo S, Leegte B, Mulder I, vd Veen AY, vd Hout AH, Wiersma TJ, van Essen AJ. Tan-Sindhunata G, et al. Among authors: castedo s. Am J Med Genet. 2000 May 15;92(2):147-52. Am J Med Genet. 2000. PMID: 10797441

3

Eleven novel APC mutations identified in Portuguese FAP families.

Isidro G, Matos P, Almeida S, Claudino S, Marshall B, Soares J, Leite J, Regateiro F, Brito MJ, Giria J, Castro C, Ramos J, Novais L, Morna H, Medeira A, Castedo S, Boavida MG. Isidro G, et al. Among authors: castedo s. Hum Mutat. 2000 Aug;16(2):178. doi: 10.1002/1098-1004(200008)16:2<178::AID-HUMU15>3.0.CO;2-#. Hum Mutat. 2000. PMID: 10923044

4

Three cases of mosaicism for balanced reciprocal translocations.

Leegte B, Sikkema-Raddatz B, Hordijk R, Bouman K, van Essen T, Castedo S, de Jong B. Leegte B, et al. Among authors: castedo s. Am J Med Genet. 1998 Oct 12;79(5):362-5. Am J Med Genet. 1998. PMID: 9779802 Review.

5

Bilateral split hand/foot malformation and inv(7)(p22q21.3).

Cobben JM, Verheij JB, Eisma WH, Robinson PH, Zwierstra RP, Leegte B, Castedo S. Cobben JM, et al. Among authors: castedo s. J Med Genet. 1995 May;32(5):375-8. doi: 10.1136/jmg.32.5.375. J Med Genet. 1995. PMID: 7616545 Free PMC article.

6

Three novel APC gene mutations in Portuguese FAP kindreds.

Marshall B, Isidro G, Carvalhas R, Veiga I, Castedo S, Soares J, Boavida MG. Marshall B, et al. Among authors: castedo s. Hum Mutat. 1996;8(4):395-6. doi: 10.1002/humu.1380080405. Hum Mutat. 1996. PMID: 8956059 No abstract available.

7

Four novel MSH2 / MLH1 gene mutations in portuguese HNPCC families.

Isidro G, Veiga I, Matos P, Almeida S, Bizarro S, Marshall B, Baptista M, Leite J, Regateiro F, Soares J, Castedo S, Boavida MG. Isidro G, et al. Among authors: castedo s. Hum Mutat. 2000 Jan;15(1):116. doi: 10.1002/(SICI)1098-1004(200001)15:1<116::AID-HUMU24>3.0.CO;2-Q. Hum Mutat. 2000. PMID: 10612836

8

Pathological exon skipping in an HNPCC proband with MLH1 splice acceptor site mutation.

Clarke LA, Veiga I, Isidro G, Jordan P, Ramos JS, Castedo S, Boavida MG. Clarke LA, et al. Among authors: castedo s. Genes Chromosomes Cancer. 2000 Dec;29(4):367-70. Genes Chromosomes Cancer. 2000. PMID: 11066084

9

Translocation t(5;19): a recurrent change in thyroid follicular adenoma.

Roque L, Castedo S, Clode A, Soares J. Roque L, et al. Among authors: castedo s. Genes Chromosomes Cancer. 1992 Jun;4(4):346-7. doi: 10.1002/gcc.2870040413. Genes Chromosomes Cancer. 1992. PMID: 1377944

10

E-Cadherin (CDH1) and p53 rather than SMAD4 and Caspase-10 germline mutations contribute to genetic predisposition in Portuguese gastric cancer patients.

Oliveira C, Ferreira P, Nabais S, Campos L, Ferreira A, Cirnes L, Alves CC, Veiga I, Fragoso M, Regateiro F, Dias LM, Moreira H, Suriano G, Machado JC, Lopes C, Castedo S, Carneiro F, Seruca R. Oliveira C, et al. Among authors: castedo s. Eur J Cancer. 2004 Aug;40(12):1897-903. doi: 10.1016/j.ejca.2004.04.027. Eur J Cancer. 2004. PMID: 15288293 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

89 results

Search Page

Filters