Nunes M - Search Results

1

Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1.

Scherer SW, Poorkaj P, Allen T, Kim J, Geshuri D, Nunes M, Soder S, Stephens K, Pagon RA, Patton MA, et al. Scherer SW, et al. Among authors: nunes m. Am J Hum Genet. 1994 Jul;55(1):12-20. Am J Hum Genet. 1994. PMID: 8023840 Free PMC article. Review.

2

Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly.

Scherer SW, Poorkaj P, Massa H, Soder S, Allen T, Nunes M, Geshuri D, Wong E, Belloni E, Little S, et al. Scherer SW, et al. Among authors: nunes m. Hum Mol Genet. 1994 Aug;3(8):1345-54. doi: 10.1093/hmg/3.8.1345. Hum Mol Genet. 1994. PMID: 7987313

3

A contiguous gene deletion syndrome at 7q21-q22 and implications for a relationship between isolated ectrodactyly and syndromic ectrodactyly.

Nunes ME, Pagon RA, Disteche CJ, Evans JP. Nunes ME, et al. Clin Dysmorphol. 1994 Oct;3(4):277-86. Clin Dysmorphol. 1994. PMID: 7894731

4

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: nunes me. 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

5

A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.

Nunes ME, Schutt G, Kapur RP, Luthardt F, Kukolich M, Byers P, Evans JP. Nunes ME, et al. Hum Mol Genet. 1995 Nov;4(11):2165-70. doi: 10.1093/hmg/4.11.2165. Hum Mol Genet. 1995. PMID: 8589697

6

Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome.

Veitia RA, Nunes M, Quintana-Murci L, Rappaport R, Thibaud E, Jaubert F, Fellous M, McElreavey K, Gonçalves J, Silva M, Rodrigues JC, Caspurro M, Boieiro F, Marques R, Lavinha J. Veitia RA, et al. Among authors: nunes m. Am J Hum Genet. 1998 Sep;63(3):901-5. doi: 10.1086/302023. Am J Hum Genet. 1998. PMID: 9718353 Free PMC article. No abstract available.

7

Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene.

Ion R, Telvi L, Chaussain JL, Barbet JP, Nunes M, Safar A, Réthoré MO, Fellous M, McElreavey K. Ion R, et al. Among authors: nunes m. Hum Genet. 1998 Feb;102(2):151-6. doi: 10.1007/s004390050669. Hum Genet. 1998. PMID: 9521582

8

Hypertelorism and hypospadias associated with a de novo apparently balanced translocation between 8q22.3-23 and 20p13.

Tar A, Ion A, Sólyom J, Györvári B, Stephenson C, Barbaux S, Nunes M, Fellous M, McElreavey K. Tar A, et al. Among authors: nunes m. Am J Med Genet. 1997 Jan 20;68(2):231-5. doi: 10.1002/(sici)1096-8628(19970120)68:2<231::aid-ajmg22>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9028465

9

Report of the Third International Workshop on Human Chromosome 8 Mapping. San Antonio, Texas, October 25-27, 1996.

Leach RJ, Banga SS, Ben-Othame K, Chughtai S, Clarke R, Daiger SP, Kolehmainen J, Kumar S, Kuo M, Macoska J, Mada N, Naylor SL, Nunes M, O'Connell P, Pebusque MJ, Pekkel V, Porter CJ, Simons CT, Sohocki MM, Trapman J, Wells D, Westbrook C, Wood S. Leach RJ, et al. Among authors: nunes m. Cytogenet Cell Genet. 1996;75(2-3):71-84. doi: 10.1159/000134460. Cytogenet Cell Genet. 1996. PMID: 9040775 No abstract available.

10

Deletions of distal 9p associated with 46,XY male to female sex reversal: definition of the breakpoints at 9p23.3-p24.1.

Veitia R, Nunes M, Brauner R, Doco-Fenzy M, Joanny-Flinois O, Jaubert F, Lortat-Jacob S, Fellous M, McElreavey K. Veitia R, et al. Among authors: nunes m. Genomics. 1997 Apr 15;41(2):271-4. doi: 10.1006/geno.1997.4648. Genomics. 1997. PMID: 9143505

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