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- 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
- Red Flags and Rules of Thumb: Sorting out Developmental Delays
- Evaluation of Macrocephaly
- Familial Scaphocephaly Syndrome Caused by a Novel Mutation in The
- The Ontogeny of Robin Sequence
- The Importance of Head Circumference: When to Reassure, When to Monitor, When to Refer?
- Role of the Dysmorphologic Evaluation in the Child with Developmental Delay
- Birth Defects Surveillance a Manual for Programme Managers
- Syndrome J Med Genet: First Published As 10.1136/Jmg.31.8.635 on 1 August 1994
- Review of Smallpox Vaccines
- Congenital CNS Anomalies (General)
- Report National Birth Defect Registry April 2009 Countofbirth Defect ID
- Syndrome Spotter Syndrome Spotter
- Macrocephaly–Cutis Marmorata Telangiectatica Congenita Syndrome” Report of 12 New Cases and Support for Revising the Name to Macrocephaly–Capillary Malformations
- Prevalence and Incidence of Rare Diseases: Bibliographic Data
- Prevalence and Incidence of Rare Diseases
- Etiologies Related to Deafblindness and Hear Ing Loss This Is a List of Syndromes and Conditions That May Cause a Combined Vision and DEAFBLINDNESS Hearing Loss
- Thieme: Handbook of Pediatric Orthopedics
- Megalencephaly Polymicrogyria Polydactyly Hydrocephalus (MPPH): a Case Report and Review of Literature
- A Clinical Review and Introduction of the Diagnostic Algorithm For
- Infant Head Shape Evaluation Savannah Brown MPAS, PA-C Elizabeth Wetz MS, MPAS, PA-C
- Neural Tube Defects Continue to Be the Leading Foetal Malformation
- MACDP's Birth Defects and Genetic Diseases Branch 6-Digit Code