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Brachydactyly

  • A Novel Locus for Brachydactyly Type A1 on Chromosome 5P13.3-P13.2 C M Armour, M E Mccready, a Baig,Agwhunter, D E Bulman

    A Novel Locus for Brachydactyly Type A1 on Chromosome 5P13.3-P13.2 C M Armour, M E Mccready, a Baig,Agwhunter, D E Bulman

  • The Genetic Heterogeneity of Brachydactyly Type A1: Identifying the Molecular Pathways

    The Genetic Heterogeneity of Brachydactyly Type A1: Identifying the Molecular Pathways

  • Genetics of Congenital Hand Anomalies

    Genetics of Congenital Hand Anomalies

  • Orphanet Journal of Rare Diseases Biomed Central

    Orphanet Journal of Rare Diseases Biomed Central

  • Craniofacial Development After Three Different Palatoplasties in Children Born with Isolated Cleft Palate

    Craniofacial Development After Three Different Palatoplasties in Children Born with Isolated Cleft Palate

  • Blueprint Genetics Craniosynostosis Panel

    Blueprint Genetics Craniosynostosis Panel

  • Free PDF Download

    Free PDF Download

  • MR Imaging of Fetal Head and Neck Anomalies

    MR Imaging of Fetal Head and Neck Anomalies

  • IIA O B Dominant Trait

    IIA O B Dominant Trait

  • Robinow Syndrome M a Patton, a R Afzal

    Robinow Syndrome M a Patton, a R Afzal

  • Identifying the Misshapen Head: Craniosynostosis and Related Disorders Mark S

    Identifying the Misshapen Head: Craniosynostosis and Related Disorders Mark S

  • Brachydactyly

    Brachydactyly

  • Review Article Cleidocranial Dysplasia: Clinical and Molecular Genetics

    Review Article Cleidocranial Dysplasia: Clinical and Molecular Genetics

  • Differential Diagnosis of Complex Conditions in Paleopathology: a Mutational Spectrum Approach by Elizabeth Lukashal a Thesis

    Differential Diagnosis of Complex Conditions in Paleopathology: a Mutational Spectrum Approach by Elizabeth Lukashal a Thesis

  • A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita

    A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita

  • Crouzono-Dermo-Skeletal Syndrome, Crouzon Syndrome with Acanthosis Nigricans Syndrome

    Crouzono-Dermo-Skeletal Syndrome, Crouzon Syndrome with Acanthosis Nigricans Syndrome

  • Poland-Mobius Syndrome

    Poland-Mobius Syndrome

  • EUROCAT Syndrome Guide

    EUROCAT Syndrome Guide

Top View
  • Brachydactyly Type A1
  • Anaesthesia for a Child with Cleidocranial Dysplasia
  • Craniosynostosis
  • Dual Novel Mutations in SLC26A2 in Two Siblings with Multiple
  • 25 Cleidocranial Dysplasia
  • Blueprint Genetics Arthrogryposes Panel
  • Genetic Syndromes Associated with Craniosynostosis
  • Brachydactyly and Polydactyly with Ridge Hypoplasia
  • Brachydactyly A-1 Mutations Restricted to the Central Region of the N-Terminal Active Fragment of Indian Hedgehog
  • Cystic Kidneys in a Patient with Craniofacial Abnormalities
  • (Multiple Congenital Contractures): Diagnostic Approach to Etiology, Classification, Genetics, and General Principles
  • A Rare Case of Poland's Syndrome
  • Cukurova Medical Journal Crouzon Syndrome in Two Siblings
  • Craniosynostosis Syndromes Sequencing
  • Mobius Syndrome with Poland's Anomaly*
  • Blueprint Genetics Micromelic Dysplasia Panel
  • Review of X-Linked Syndromes with Arthrogryposis Or Early Contractures—Aid to Diagnosis and Pathway Identification Jesse M
  • Blueprint Genetics Brachydactyly / Syndactyly Panel


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