Robin sequence and oligodactyly in mother and son
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference13 articles.
1. (1949): Congenital deformities of the upper extremities. Cophenhagen, Ejnar Munksgard.
2. Pierre Robin sequence and hyperphalangy?a genetic entity
3. Robin's Syndrome
4. U-shaped palatal defect in the Robin anomalad: Developmental and clinical relevance
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1. Self-Meaning of Oligodactyly: Health Communication Study of People with Oligodactyly in the Village of Ulutaue, South Sulawesi, Indonesia;Integrative Psychological and Behavioral Science;2020-06-10
2. Unilateral Hand Oligodactyly: Prenatal Diagnosis With 3-Dimensional Sonography;Journal of Ultrasound in Medicine;2012-11
3. Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH;Human Molecular Genetics;2012-06-12
4. Exome sequencing identifies the cause of a mendelian disorder;Nature Genetics;2009-11-13
5. REFERENCES (GAMUTS);Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007
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