PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly Corresponding author

Por um escritor misterioso

Descrição

Rubinstein-Taybi Syndrome (RSTS) is a rare multiple congenital anomaly syndrome. Only 250 cases have been described in medical literature. We hereby present a 10-month-old male child with characteristic facial features and hand and feet anomalies.
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
PDF) Rubinstein-Taybi syndrome: a rare case report of a female
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
Clinical exome sequencing identifies novel CREBBP variants in 18
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
PDF) Rubinstein-Taybi syndrome medical guidelines
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
Clinical exome sequencing identifies novel CREBBP variants in 18
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
Rubinstein‐Taybi Syndrome in a Fetus: Contribution of 2‐ and 3
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
Hedgehog signaling update - Cohen Jr. - 2010 - American Journal of
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
Rubinstein-Taybi Syndrome: A case report
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
Deciphering the mutational signature of congenital limb
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral  postaxial polydactyly Corresponding author
Diagnosis of Menke‐Hennekam syndrome by prenatal whole exome
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