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OpenAlex topic

Congenital limb and hand anomalies

This page lists works and academicians tagged with an OpenAlex topic. It is not a YÖKSİS primary or secondary field.

OpenAlex 1,373 works 7 author topics

Works

1,373 works

  1. p300 CBP and cancer 2004
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.8%

    No abstract yet.

  2. Disruption of a long range cis acting regulator for Shh causes preaxial polydactyly 2002
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.9%

    Preaxial polydactyly (PPD) is a common limb malformation in human. A number of polydactylous mouse mutants indicate that misexpression of Shh is a common requirement for generating extra digits. Here we identify a translocation breakpoint in a PPD patient and a transgenic insertion site in the polydactylous mouse muta…

  3. Fetal development of the hand digits and digit ratio 2D 4D 2006
    YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 98.7%

    No abstract yet.

  4. Fetal development of the hand digits and digit ratio 2D 4D 2006
    YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 98.7%

    No abstract yet.

  5. Fetal development of the hand digits and digit ratio 2D 4D 2006
    YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 98.7%

    No abstract yet.

  6. Fetal development of the hand digits and digit ratio 2D 4D 2006
    YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 98.5%

    No abstract yet.

  7. p63 Gene Mutations in EEC Syndrome Limb Mammary Syndrome and Isolated Split Hand Split Foot Malformation Suggest a Genotype Phenotype Correlation 2001
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.3%

    No abstract yet.

  8. Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome 2000
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 97.6%

    No abstract yet.

  9. Mutations in PIEZO2 cause Gordon syndrome Marden walker syndrome and Distal Arthrogryposis 5 2014
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.6%

    No abstract yet.

  10. LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome 2010
    OpenAlex top 10% OpenAlex 98.4%

    No abstract yet.

  11. LRP4 Mutations Alter Wnt Catenin Signaling and Cause Limb and Kidney Malformations in Cenani Lenz Syndrome 2010
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 98.4%

    No abstract yet.

  12. Genomic structure of HOXD13 gene a nine polyalanine duplication causes synpolydactyly in two unrelated families 1995
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 1% OpenAlex 99.0%

    Synpolydactyly (SPD) is a limb malformation that shows a characteristic manifestation in both hands and feet. This condition is inherited as an autosomal dominant trait with reduced penetrance. We have recently mapped this locus centromeric to the HOXD8 intragenic marker and suggested the HOXD13 gene as a potential ca…

Academicians

7 academicians