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Macrocephaly

  • Pfeiffer Syndrome Type II Discovered Perinatally

    Pfeiffer Syndrome Type II Discovered Perinatally

  • Megalencephaly and Macrocephaly

    Megalencephaly and Macrocephaly

  • Genetics of Congenital Hand Anomalies

    Genetics of Congenital Hand Anomalies

  • Macrocephaly Information Sheet 6-13-19

    Macrocephaly Information Sheet 6-13-19

  • Sotos Syndrome

    Sotos Syndrome

  • (12) Patent Application Publication (10) Pub. No.: US 2010/0210567 A1 Bevec (43) Pub

    (12) Patent Application Publication (10) Pub. No.: US 2010/0210567 A1 Bevec (43) Pub

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

    Identifying the Misshapen Head: Craniosynostosis and Related Disorders Mark S

  • Bagatelle Cassidy Syndrome: Macrocephaly

    Bagatelle Cassidy Syndrome: Macrocephaly

  • RIN2 Deficiency Results in Macrocephaly, Alopecia, Cutis Laxa

    RIN2 Deficiency Results in Macrocephaly, Alopecia, Cutis Laxa

  • Congenital Anomalies and in Utero Antiretroviral Exposure in Human Immunodeficiency Virus– Exposed Uninfected Infants

    Congenital Anomalies and in Utero Antiretroviral Exposure in Human Immunodeficiency Virus– Exposed Uninfected Infants

  • Improving Diagnosis and Treatment of Craniofacial Malformations Utilizing Animal Models

    Improving Diagnosis and Treatment of Craniofacial Malformations Utilizing Animal Models

  • Spondylocostal Dysplasia and Neural Tube Defects

    Spondylocostal Dysplasia and Neural Tube Defects

  • EUROCAT Syndrome Guide

    EUROCAT Syndrome Guide

  • The First Neurosurgical Analysis of 8 Korean Children with Sotos Syndrome

    The First Neurosurgical Analysis of 8 Korean Children with Sotos Syndrome

  • Subject Index to Abstracts

    Subject Index to Abstracts

  • A Survey of Phenotypic Features in Juvenile Polyposis J Med Genet: First Published As 10.1136/Jmg.35.6.476 on 1 June 1998

    A Survey of Phenotypic Features in Juvenile Polyposis J Med Genet: First Published As 10.1136/Jmg.35.6.476 on 1 June 1998

  • Clinical Images a Quarterly Column

    Clinical Images a Quarterly Column

  • Excluded Conditions

    Excluded Conditions

Top View
  • Guidelines for Researchers Using Data
  • Birth Defects Surveillance a Manual for Programme Managers
  • Syndrome of Megalencephaly, Polydactyly, and Polymicrogyria Lacking Frank Hydrocephalus, CASE REPORT with Associated MR Imaging Findings
  • Children with Spina Bifida and Hydrocephalus in Africa: Can
  • Genetic Disorders Associated with Macrocephaly
  • 7.1 Birth Defects Code List
  • Craniosynostosis and Related Disorders Mark S
  • Guidelines for Conducting Birth Defects Surveillance
  • Hereditary Disorders of Connective Tissue: a Guide to the Emerging Differential Diagnosis Maureen Murphy-Ryan, BS1, Apostolos Psychogios, MD2, and Noralane M
  • Review of X-Linked Syndromes with Arthrogryposis Or Early Contractures—Aid to Diagnosis and Pathway Identification Jesse M
  • Craniosynostosis HAIDAR KABBANI, M.D., and TALKAD S
  • ICD-10 Coding Manual List of All Reportable Congenital Malformations
  • Macrocephaly–Cutis Marmorata Telangiectatica Congenita Syndrome” Report of 12 New Cases and Support for Revising the Name to Macrocephaly–Capillary Malformations
  • A Review of Extraaxial Developmental Venous Anomalies of the Brain
  • Ciliopathies
  • Blueprint Genetics Macrocephaly / Overgrowth Syndrome Panel
  • Autosomal Dominant Diseases Are Too Often Overlooked in the Parents Of
  • Macrocephaly, Increased Intracranial Pressure, and Hydrocephalus in the Infant and Young Child Alexandra T


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