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- In-Depth Investigations of Adolescents and Adults with Holoprosencephaly Identify Unique Characteristics
- Surveillance of Microcephaly Webinar Transcript
- Holoprosencephaly
- The Deceptive Family Tree: Genetic Counseling Complexities in Holoprosencephaly Paul Kruszka, MD, MPH Margaret Menzel, MS, CGC Goals and Objectives
- Schizencephaly Revisited
- Cephaloceles and Related Malformations
- Holoprosencephaly Classified by Computed Tomography
- Birth Defects Surveillance Training Facilitator's Guide
- Genetic Abnormalities in Prenatally Diagnosed Central Nervous System Malformations Ting YH the Chinese University of Hong Kong, Hong Kong, Hong Kong
- ICD-10 Coding Manual List of All Reportable Congenital Malformations
- A CRISPR-Cas9–Engineered Mouse Model for GPI-Anchor Deficiency Mirrors Human Phenotypes and Exhibits Hippocampal Synaptic Dysfunctions
- Microcephaly
- Malformations of Cortical Development’ in the Pediatric Age Group
- Holoprosencephaly-Polydactyly ('Pseudotrisomy 13') Syndrome: a Syndrome with Features of Hydrolethalus and Smith-Lemli-Opitz Syndromes
- 23 Weeks Scan Copyright 2002 © by the Authors, ISUOG & Fetal Medicine Foundation, London
- Holoprosencephaly: a Rare Finding in Mosaic Trisomy 9 Syndrome
- Fetal Brain MRI Findings and Neonatal Outcome of Common Diagnosis at A
- Cebocephaly, Alobar Holoprosencephaly, Spina
- The Neonate Was Born with Holoprosencephaly Reza Saeidi1, Abdolhosein Abasi2*
- Congenital CNS Anomalies (General)
- Unilateral Closed-Lip Schizencephaly
- Non-Human Primate Models to Investigate Mechanisms of Infection-Associated Fetal and Pediatric Injury, Teratogenesis and Stillbirth
- Management of Children with Holoprosencephaly
- Holoprosencephaly
- New Findings for Phenotype-Genotype Correlations in a Large European
- Pediatric Neuroradiology Congenital Brain Anomalies for the ABR Core Exam
- In Utero MR Imaging of Fetal Holoprosencephaly: a Structured Approach to Diagnosis and Classification
- Holoprosencephaly: Prenatal Sonographic Diagnosis
- Holoprosencephaly Information Sheet 6-10-19
- The Acrocallosal Syndrome
- Blueprint Genetics Holoprosencephaly Panel