4 Newborn with Rubinstein-Taybi syndrome showing microcephaly
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Rubinstein‐Taybi Syndrome in a Fetus: Contribution of 2‐ and 3‐Dimensional Ultrasonography - Cardalliac - 2018 - Journal of Ultrasound in Medicine - Wiley Online Library
Hyperinsulinism in an individual with an EP300 variant of Rubinstein‐Taybi syndrome - Wild - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library
Born with Rubinstein-Taybi Syndrome (RTS), Braxton and Family are Full of Hope - Global Genes
MICROCEPHALY jo.pptx
Genes, Free Full-Text
Seckel Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a frameshift mutation in the CREBBP gene
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Causes of microcephaly.
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the opening
Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus
Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus
4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal
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