Patient Stories Rubinstein-Taybi Syndrome
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Children who have Rubinstein-Taybi syndrome can, and do, grow and thrive. Find stories of hope from our patients who are living life to the fullest.
Patient Stories Rubinstein-Taybi Syndrome
Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients
Rubinstein taybi syndrome
DBMCI MDS (Formerly MDS Experts) on Instagram: RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated with deletions of the short arm of ch 16. Clinical Features: • Mental retardation • Broad thumbs •
Silas : Rubinstein-Taybi Syndrome » SWEET NECTAR SOCIETY
Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
Rubinstein-Taybi Syndrome: A case report
IJMS, Free Full-Text
Meet Kate: She's 1 in 100,000 because of RTS
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Genes, Free Full-Text
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