Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
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Pediatric intestinal motility disordersMultiple endocrine neoplasia type 2: an overviewSchwann cell hamartoma: case report.Recombinant leukemia inhibitory factor suppresses human medullary thyroid carcinoma cell line xenografts in mice.Multiple endocrine neoplasias type 2B and RET proto-oncogene.Painful Hip Leading to the Diagnosis of MEN 2B Syndrome.Reactive hyperplasias,precancerous and malignant lesions of the oral mucosa.Mucosal Schwann cell "Hamartoma": a new entity?Recombination as a mechanism for sporadic mutation in the surfactant protein-C geneA family presenting with multiple endocrine neoplasia type 2B: A case report.A Case of Multiple Endocrine Neoplasia Type 2B and Gangliomatosis of Gastrointestinal Tract.Hereditary and familial thyroid tumours.Small intestinal ganglioneuromatosis in a dog
P2860
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P2860
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
description
2000 nî lūn-bûn
@nan
2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@ast
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@en
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@nl
type
label
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@ast
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@en
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@nl
prefLabel
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@ast
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@en
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@nl
P1433
P1476
Multiple endocrine neoplasia type 2B--genetic basis and clinical expression.
@en
P2093
P304
P356
10.1016/S0960-7404(00)00038-4
P577
2000-11-01T00:00:00Z