Research map: Compound Heterozygosity for Hb Port Phillip and the –α 3.7 Deletion Leads to Persistent Hypoxemia in a Chinese Pediatric Family

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  1. Hemoglobin Variants: Biochemical Properties and Clinical Correlates · Christopher S. Thom · 2013 · 342 citations · Cited by this paper
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  22. HPLC first approach in detecting thalassemia and other common hemoglobinopathies is more cost and time effective · Sundar Periyavan · 2025 · 7 citations · Cited by this paper
  23. Compounded with hemoglobin Port Phillip and ‐α4.2 or ‐‐SEA deletions were identified in Chinese population · Li Lin Du · 2021 · 7 citations · Cited by this paper
  24. Hb Treviso [α91(FG3)Leu→Phe (α2)]: A New Slightly Unstable Hemoglobin Variant with Moderately Decreased Oxygen Affinity · Giuseppina Barberio · 2013 · 4 citations · Cited by this paper
  25. Analysis of the Haematological Phenotype and Molecular Characteristics of Rare Abnormal Haemoglobin · Yanfen Ge · 2024 · 4 citations · Cited by this paper
  26. Hemoglobin Alpha Chain Variant Zara Associated With Familial Asymptomatic Hypoxemia · Anthony Pasquarella · 2022 · 3 citations · Cited by this paper
  27. Identification of Novel Hb Guiyang [HBA2: c.151C > A α2 50 (CE8) His- Asn] and Phenotype- Genotype Correlation of Abnormal Hemoglobins in Guizhou, Southwest China · Yaping Chen · 2024 · 1 citation · Cited by this paper
  28. Hemoglobin J-Auckland: a clinically silent low oxygen affinity variant presenting with persistent asymptomatic hypoxemia at high altitude · Ali Alsuheel Asseri · 2024 · 1 citation · Cited by this paper
  29. A long-lasting low oxygen saturation hiding Titusville hemoglobin diagnosis in a premature 14-month-old child – case report · Maria Francesca Patria · 2025 · 1 citation · Cited by this paper

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