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单词
hegglin's anomaly
释义
Hegglin's anomaly
Heg·glin's anomaly
(hĕg′lĭnz)
n.
A hereditary disorder characterized by basophilic structures in most granulocytes, faulty maturation of platelets, and thrombocytopenia. Also called
May-Hegglin anomaly
.
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guanine nucleotide-binding protein g(i)/g(s)/g(t) subunit beta-3
guanine nucleotide binding protein (g protein), beta 5
guanine nucleotide binding protein (g protein), beta polypeptide 1
guanine nucleotide binding protein (g protein), beta polypeptide 2
guanine nucleotide binding protein (g protein), beta polypeptide 3
guanine nucleotide binding protein (g protein), beta polypeptide 4
guanine nucleotide-binding protein g(s) subunit alpha isoforms xlas
guanine nucleotide binding proteins
guanine nucleotide-binding protein subunit beta-2-like 1
guanine nucleotide-binding protein subunit beta-4
guanine nucleotide-binding protein subunit beta-5
guanine nucleotide exchange factor
guanine-nucleotide exchange factor
guanine nucleotide exchange factor lbc
guanine nucleotide exchange factor vav2
guanine nucleotide exchange factor vav3
guanine nucleotide regulatory protein
guanine nucleotide-releasing protein
guanine nucleotides
guanine ribonucleotide
guanine-thymine
guanine, thymine, cytosine, adenine
guanine-uracil-guanine
guanin (fish)
guanite
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更新时间:2026/6/30 9:34:56