Sajid Malik

Summary

Affiliation: Philipps University
Country: Germany

Publications

  1. Abbasi A, Paparidis Z, Malik S, Bangs F, Schmidt A, Koch S, et al. Human intronic enhancers control distinct sub-domains of Gli3 expression during mouse CNS and limb development. BMC Dev Biol. 2010;10:44 pubmed publisher
    ....
  2. Malik S, Girisha K, Wajid M, Roy A, Phadke S, Haque S, et al. Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences. BMC Med Genet. 2007;8:78 pubmed
    ..It is the first molecular evidence supporting the hypothesis that expansion of < or = 6 alanine residues in the HOXD13 polyalanine repeat is not associated with the SPD1 phenotype. ..
  3. Malik S, Arshad M, Amin Ud Din M, Oeffner F, Dempfle A, Haque S, et al. A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani origin. Am J Med Genet A. 2004;126A:61-7 pubmed
    ..We show that the phenotype in our family is not linked to chromosomal regions 2q34-q36, 2q31, and 6q22-q23 encompassing loci for syndactyly types I, II, and III...
  4. Malik S, Percin F, Ahmad W, Percin S, Akarsu N, Koch M, et al. Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3. Am J Med Genet A. 2005;134:404-8 pubmed
    ....
  5. Malik S, Ahmad W, Grzeschik K, Koch M. A simple method for characterising syndactyly in clinical practice. Genet Couns. 2005;16:229-38 pubmed
    ..It might encourage clinicians to report families that are still unclassifed and thus, helping to extend and improve the existing classification system...
  6. Malik S, Grzeschik K. Synpolydactyly: clinical and molecular advances. Clin Genet. 2008;73:113-20 pubmed publisher
    ..Our lumping and splitting scheme for SPD phenotypic variants could be useful for the understanding of this interesting malformation...

Detail Information

Publications6

  1. Abbasi A, Paparidis Z, Malik S, Bangs F, Schmidt A, Koch S, et al. Human intronic enhancers control distinct sub-domains of Gli3 expression during mouse CNS and limb development. BMC Dev Biol. 2010;10:44 pubmed publisher
    ....
  2. Malik S, Girisha K, Wajid M, Roy A, Phadke S, Haque S, et al. Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences. BMC Med Genet. 2007;8:78 pubmed
    ..It is the first molecular evidence supporting the hypothesis that expansion of < or = 6 alanine residues in the HOXD13 polyalanine repeat is not associated with the SPD1 phenotype. ..
  3. Malik S, Arshad M, Amin Ud Din M, Oeffner F, Dempfle A, Haque S, et al. A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani origin. Am J Med Genet A. 2004;126A:61-7 pubmed
    ..We show that the phenotype in our family is not linked to chromosomal regions 2q34-q36, 2q31, and 6q22-q23 encompassing loci for syndactyly types I, II, and III...
  4. Malik S, Percin F, Ahmad W, Percin S, Akarsu N, Koch M, et al. Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3. Am J Med Genet A. 2005;134:404-8 pubmed
    ....
  5. Malik S, Ahmad W, Grzeschik K, Koch M. A simple method for characterising syndactyly in clinical practice. Genet Couns. 2005;16:229-38 pubmed
    ..It might encourage clinicians to report families that are still unclassifed and thus, helping to extend and improve the existing classification system...
  6. Malik S, Grzeschik K. Synpolydactyly: clinical and molecular advances. Clin Genet. 2008;73:113-20 pubmed publisher
    ..Our lumping and splitting scheme for SPD phenotypic variants could be useful for the understanding of this interesting malformation...