Congenital anomalies and genetic syndromes in 173 cases of medulloblastoma

scientific article

Congenital anomalies and genetic syndromes in 173 cases of medulloblastoma is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/MPO.2950210608
P698PubMed publication ID8515724

P50authorGareth EvansQ29642643
P2093author name stringCampbell R
Birch J
Gattamaneni HR
Burnell L
P2860cites workThe incidence of Gorlin syndrome in 173 consecutive cases of medulloblastomaQ35993240
P433issue6
P921main subjectcongenital disorderQ727096
medulloblastomaQ1333608
P304page(s)433-434
P577publication date1993-01-01
P1433published inPediatric Blood & CancerQ15754342
P1476titleCongenital anomalies and genetic syndromes in 173 cases of medulloblastoma
P478volume21

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Q34312510Failure of a medulloblastoma-derived mutant of SUFU to suppress WNT signaling
Q49548506Germline SUFU mutation carriers and medulloblastoma: clinical characteristics, cancer risk and prognosis.
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Q91596369Medulloblastoma
Q81665531Medulloblastoma in the first year of life: A report of five cases
Q38791824Medulloblastoma: Tumor Biology and Relevance to Treatment and Prognosis Paradigm
Q90029728Medulloblastomas associated with an APC germline pathogenic variant share the good prognosis of CTNNB1-mutated medulloblastomas
Q34051118Molecular insight into medulloblastoma and central nervous system primitive neuroectodermal tumor biology from hereditary syndromes: a review
Q37579203Molecular variants and mutations in medulloblastoma
Q41687884Neurotrophins in cerebellar granule cell development and medulloblastoma
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Q28080220Ultra-Rare Syndromes: The Example of Rubinstein-Taybi Syndrome

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