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Trigonocephaly

  • Second Family with the Bostontype Craniosynostosis Syndrome: Novel Mutation and Expansion of the Clinical Spectrum

    Second Family with the Bostontype Craniosynostosis Syndrome: Novel Mutation and Expansion of the Clinical Spectrum

  • Dysmorphology and Dysfunction in the Brain and Calvarial Vault of Nonsyndromic Craniosynostosis

    Dysmorphology and Dysfunction in the Brain and Calvarial Vault of Nonsyndromic Craniosynostosis

  • Endoscopy-Assisted Early Correction of Single-Suture Metopic Craniosynostosis: a 19-Year Experience

    Endoscopy-Assisted Early Correction of Single-Suture Metopic Craniosynostosis: a 19-Year Experience

  • West Texas Craniofacial Center of Excellence

    West Texas Craniofacial Center of Excellence

  • Blueprint Genetics Craniosynostosis Panel

    Blueprint Genetics Craniosynostosis Panel

  • Prenatal Ultrasonography of Craniofacial Abnormalities

    Prenatal Ultrasonography of Craniofacial Abnormalities

  • MR Imaging of Fetal Head and Neck Anomalies

    MR Imaging of Fetal Head and Neck Anomalies

  • Detailed Characterization Of, and Clinical Correlations In, 10 Patients

    Detailed Characterization Of, and Clinical Correlations In, 10 Patients

  • Craniosynostosis Precision Panel Overview Indications Clinical Utility

    Craniosynostosis Precision Panel Overview Indications Clinical Utility

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

    Identifying the Misshapen Head: Craniosynostosis and Related Disorders Mark S

  • Hydrocephalus and Craniosynostosis

    Hydrocephalus and Craniosynostosis

  • Psychological Adjustment to Craniofacial Conditions (Excluding Oral Clefts): a Review of the Literature

    Psychological Adjustment to Craniofacial Conditions (Excluding Oral Clefts): a Review of the Literature

  • Craniofacial Diseases Caused by Defects in Intracellular Trafficking

    Craniofacial Diseases Caused by Defects in Intracellular Trafficking

  • A Heads up on Craniosynostosis

    A Heads up on Craniosynostosis

  • Craniofacial Syndromes: Crouzon, Apert, Pfeiffer, Saethre-Chotzen, and Carpenter Syndromes, Pierre Robin Syndrome, Hemifacial Deformity 10/4/17, 4�06 PM

    Craniofacial Syndromes: Crouzon, Apert, Pfeiffer, Saethre-Chotzen, and Carpenter Syndromes, Pierre Robin Syndrome, Hemifacial Deformity 10/4/17, 406 PM

  • Appendix 3.1 Birth Defects Descriptions for NBDPN Core, Recommended, and Extended Conditions Updated March 2017

    Appendix 3.1 Birth Defects Descriptions for NBDPN Core, Recommended, and Extended Conditions Updated March 2017

  • Metopic and Sagittal Synostosis in Greig Cephalopolysyndactyly Syndrome: five Cases with Intragenic Mutations Or Complete Deletions of GLI3

    Metopic and Sagittal Synostosis in Greig Cephalopolysyndactyly Syndrome: five Cases with Intragenic Mutations Or Complete Deletions of GLI3

  • A Guide to Understanding Craniosynostosis

    A Guide to Understanding Craniosynostosis

Top View
  • Craniosynostosis
  • Genetics of Trigonocephaly (Metopic Synostosis) Information for Parents
  • Craniosynostosis CRANIOSYNOSTOSIS
  • Mac Med Review 2016; 70(2): 99-103 99
  • Mutations in TFAP2B and Previously Unimplicated Genes of the BMP, Wnt, and Hedgehog Pathways in Syndromic Craniosynostosis
  • Congenital Cranial Anomalies and Cleft Palate Craniofacial Surgery
  • Metopic Craniosynostosis and Hydrocephalus in a Premature Opioid Dependent Baby
  • Birth Defects Surveillance a Manual for Programme Managers
  • Opitz C Syndrome: Trigonocephaly, Mental Retardation and Craniofacial Dysmorphism
  • Opitz C Syndrome: Trigonocephaly, Mental Retardation and Craniofacial Dysmorphism
  • 7.1 Birth Defects Code List
  • Craniosynostosis and Related Disorders Mark S
  • Congenital Malformations Notice
  • Guidelines for Conducting Birth Defects Surveillance
  • Sciencedirect
  • Mild Trigonocephaly Associated with Microcephaly: Surgical Outcomes for 15 Cases
  • Congenital Craniofacial Deformities: Spectrum of Multidetector Computed Tomographic Findings
  • Craniosynostosis and Syndactyly: Deletion Phenotype *


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