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De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndromeA novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 genePrenatal ultrasonographic and molecular diagnosis of Apert syndromePathology forum: quiz case 4. Diagnosis: synovial chondromatosis of the TMJPathology quiz case 1. Diagnosis: carcinoid tumor of the middle ear
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description
onderzoeker
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researcher
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հետազոտող
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name
W Jiang
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W Jiang
@en
W Jiang
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W Jiang
@nl
W Jiang
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type
label
W Jiang
@ast
W Jiang
@en
W Jiang
@es
W Jiang
@nl
W Jiang
@sl
prefLabel
W Jiang
@ast
W Jiang
@en
W Jiang
@es
W Jiang
@nl
W Jiang
@sl
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P496
0000-0002-3916-8826