Cytogenetic and CGH studies of four neuroendocrine tumors and tumor-derived cell lines of a patient with multiple endocrine neoplasia type 1.

scientific article published in July 1999

Cytogenetic and CGH studies of four neuroendocrine tumors and tumor-derived cell lines of a patient with multiple endocrine neoplasia type 1. is …
instance of (P31):
scholarly articleQ13442814

External links are
P698PubMed publication ID10375592

P50authorBruno NiederleQ39450690
P2093author name stringPfragner R
Behmel A
Henn T
Wirnsberger G
Kaserer K
Sigl E
Weinhausl A
P4510describes a project that usesLOHG-NSAQ54902883
LOHG-FQ54902880
LOHG-IQ54902881
LOHG-LQ54902882
P433issue1
P921main subjectmultiple endocrine neoplasiaQ1553018
cell lineQ21014462
P304page(s)41-51
P577publication date1999-07-01
P1433published inInternational Journal of OncologyQ6051527
P1476titleCytogenetic and CGH studies of four neuroendocrine tumors and tumor-derived cell lines of a patient with multiple endocrine neoplasia type 1.
P478volume15

Reverse relations

described by source (P1343)
Q54902880LOHG-F
Q54902881LOHG-I
Q54902882LOHG-L
Q54902883LOHG-NSA

cites work (P2860)
Q9003774018F-FDOPA PET/CT accurately identifies MEN1-associated pheochromocytoma
Q35842229Putative tumor suppressor loci at 6q22 and 6q23-q24 are involved in the malignant progression of sporadic endocrine pancreatic tumors

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