The Turkish Journal of Pediatrics
Smilar Issues: 14 Record Found
Congenital cardiac defects with 22q11 deletion Abstract Similar Articles Mail to Editor Asymmetric crying facies associated with congenital hypoparathyroidism and 22q11 deletion Abstract Similar Articles Mail to Editor Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy Abstract Similar Articles Mail to Editor A report of a patient with duplication of 7p13→pter and deletion of 2p23→pter due to a maternal 2p;7p translocation Abstract Similar Articles Mail to Editor Two new cases with Pearson syndrome and review of Hacettepe experience Abstract Similar Articles Mail to Editor A case with a ring chromosome 22 Abstract Similar Articles Mail to Editor A Rare Case of 2q37 Microdeletion with Albright Hereditary Osteodystrophy-Like Phenotype Abstract Similar Articles Mail to Editor Prenatally Diagnosed Case of 22q11.2 Deletion Syndrome Associated with Pulmonary Artery Aneurysm Abstract Similar Articles Mail to Editor The MEFV gene and clonal myeloid disorders Abstract Similar Articles Mail to Editor Jacobsen Syndrome without Thrombocytopenia: A Case Report and Review of the Literature Abstract Similar Articles Mail to Editor A Case of Sotos Syndrome with 5q35 Microdeletion and Novel Clinical Findings Abstract Similar Articles Mail to Editor Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region Abstract Similar Articles Mail to Editor The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome Abstract Similar Articles Mail to Editor Familial reciprocal non robertsonian translocation t(14;22) resulting in 22q11.2 deletion syndrome Abstract Similar Articles Mail to Editor
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