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Dysmorphic feature
Amit C, Et Al. Functional Genomics Study of Sick Neonate Affected with Copyright© Amit C, Et Al
Common Neonatal Syndromes
Dysmorphology Training Manual
Application of High-Resolution Array Comparative Genomic Hybridization in Children with Unknown Syndromic Microcephaly
Evaluation and Diagnosis of the Dysmorphic Infant
Craniofacial Features of 3Q29 Deletion Syndrome: Application of Next Generation Phenotyping Technology
Prospective Investigation of Autism and Genotype
Addressing Fetal Alcohol Spectrum Disorders (FASD)
Chromosome Syndromes Congenital Heart Defects
Use of Dysmorphology for Subgroup Classification on Autism Spectrum Disorder in Chinese Children
Development and Validation of a Measure of Dysmorphology: Useful for Autism Subgroup Classification
CDK5RAP2 Primary Microcephaly Is Associated With
The Utility of Whole Exome Sequencing in Patients with Intellectual Disability and Developmental Delay As a First-Tier Diagnostic Testing Strategy
Prospective Investigation of Autism and Genotype-Phenotype Correlations in 22Q13 Deletion Syndrome and SHANK3 Deficiency
Role of the Dysmorphologic Evaluation in the Child with Developmental Delay
HANDBOOK for Screening Visible Birth Defects at All Delivery Points
Neonatal Diagnosis of 49, XXXXY Syndrome
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Dysmorphology, Abnormal Growth and Copy Number
Évaluation Du Caryotype Moléculaire En Tant Qu'outil Diagnostique Chez
Can Psychiatric Childhood Disorders Be Due to Inborn Errors of Metabolism?