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VACTERL association
VATER/VACTERL Association in Palestinian Children: a Case Report
Holt-Oram Syndrome: a Clinical Genetic Study J Med Genet: First Published As 10.1136/Jmg.33.4.300 on 1 April 1996
Case Report Upper Limb Meromelia with Oligodactyly and Brachymesophalangy of the Foot: an Unusual Association
VACTERL/VATER Association Benjamin D Solomon
Case Reports Ultrasound Relevance in Prenatal Diagnosis of Vacterl
Early ACCESS Diagnosed Conditions List
Whole-Exome Sequencing Identifies Causative Mutations in Families
Appendix 3.1 Birth Defects Descriptions for NBDPN Core, Recommended, and Extended Conditions Updated March 2017
Genetics of Atrioventricular Canal Defects Flaminia Pugnaloni1, Maria Cristina Digilio2, Carolina Putotto1, Enrica De Luca1, Bruno Marino1 and Paolo Versacci1*
Platform Abstracts
EUROCAT Syndrome Guide
Blueprint Genetics Ciliopathy Panel
Prenatal Microarray Disorders List V19.1
Congenital Hand Anomalies and Associated Syndromes Ghazi M
Prevalence of Congenital Malformations at the “Les Orangers” Maternity and Reproductive Health Hospital of Rabat: Descriptive Study of 470 Anomalies K
Congenital Heart Defects and Ciliopathies Associated with Renal Phenotypes
Excluded Conditions
GENETIC TESTING REQUISITION Please Ship All NON-PRENATAL
Top View
What Is New in Genetics of Congenital Heart Defects?
Birth Defects Surveillance a Manual for Programme Managers
Congenital Anomalies Surveillance 2012-2013
Western Abstracts Subject Index
7.1 Birth Defects Code List
A Case of VACTERL Association
NIH Public Access Author Manuscript Am J Med Genet A
Congenital Malformations Notice
Genetic Factors in Esophageal Atresia, Tracheo
Guidelines for Conducting Birth Defects Surveillance
Congenital Anomaly Surveillance 2014-2015
P-00814 (12/2020) 4
Neonate with VACTERL Association: a Rare Entity
TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome DEBORAH A
Tetralogy of Fallot in a Child with VACTERL Association - a Case Report of Uncommon Occurrence Authors Praveen Nagula1, Anjani Kiranmayi K.1, M
Those Followed by F Indicate Figures
Sirenomelia and Severe Caudal Regression Syndrome
Oesophageal Atresia, Tracheo-Oesophageal Fistula and the VACTERL Association: Review of Genetics and Epidemiology. Charles Shaw