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Asymmetric crying facies
Genevista Microdeletion and Microduplication Syndromes
Duchenne Muscular Dystrophy (DMD)
Digeorge Syndrome
Clinical Findings in 32 Patients with 22Qll.2 Microdeletion Attended in the City of Córdoba, Argentina
Genes, Hearing, and Deafness : from Molecular Biology to Clinical Practice
D. Wangl, R. Sapolsky2,1, Spencer.1, T. Riouxl, L
IJOMCR Vol.||02||Issue||03||Page 14-17||Jul-Sep 2016
Syndrome? J Med Genet: First Published As 10.1136/Jmg.34.1.79 on 1 January 1997
View & Print the Complete Manual
Appendix 3.1 Birth Defects Descriptions for NBDPN Core, Recommended, and Extended Conditions Updated March 2015
Genevista Fetal Dysmorphology: an Indispensable Tool for Synthesis Of
7.1 Birth Defects Code List
Familial Congenital Facial Synkinesis
Congenital Malformations Notice
Cumulative Contents to Volume 25
Evaluation and Diagnosis of the Dysmorphic Infant
Hemizygous Mutations in SNAP29 Unmask Autosomal Recessive
Isolated Dysmorphologies
Top View
GENERAL PRACTICE Part 2
List Rare Diseases.Txt
13 CAN't-MISS SYNDROMES Mark J. Stephan, MD Bonnie Geneman
Adults with Genetic Syndromes and Cardiovascular Abnormalities: Clinical History and Management Angela E
13Assessment of the Dysmorphic Infant
Therapeutic and Diagnostic Agents
Velo-Cardio-Facial Syndrome
Genetics Update for the Next Ration Clinician
A Genetic, Epigenetic and Transcriptomic Study of 22Q11.2 Deletion Syndrome and Its Schizophrenia Phenotype
Common Genetic Disorders 9 6 2017 Child Neurology
Orphanet Report Series Rare Diseases Collection