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Recessive Hereditary Methemoglobinemia Type II in a Microcephalic Infant.
Clin Pediatr (Phila). 2024 Mar 4:99228241235441. doi: 10.1177/00099228241235441. Online ahead of print.
Clin Pediatr (Phila). 2024.
PMID: 38439554
No abstract available.
Persistent Cutis Marmorata Telangiectatica Congenita Associated with Isolated Hemihypertrophy and Edema Attacks.
Belgemen-Ozer T.
Belgemen-Ozer T.
Clin Pediatr (Phila). 2024 Jun;63(5):617-619. doi: 10.1177/00099228231187482. Epub 2023 Jul 18.
Clin Pediatr (Phila). 2024.
PMID: 37464812
No abstract available.
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A Very Rare Congenital Dyserythropoietic Anemia Variant-Type IV in a Patient With a Novel Mutation in the KLF1 Gene: A Case Report and Review of the Literature.
Belgemen-Ozer T, Gorukmez O.
Belgemen-Ozer T, et al.
J Pediatr Hematol Oncol. 2020 Aug;42(6):e536-e540. doi: 10.1097/MPH.0000000000001727.
J Pediatr Hematol Oncol. 2020.
PMID: 32032242
Review.
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