Results 161 to 170 of about 23,942 (228)

Hybrid neurofibroma/schwannoma in schwannomatosis-a diagnostically challenging benign peripheral nerve sheath tumour. [PDF]

Fam Cancer
Tippner D, Anokhin M, Scheffler J, Hellmann F, Plontke SK, Leisz S, Harder A.   +6 more
europepmc   +1 more source

The genotypic and family characteristics and clinical intervention of neurofibromatosis type 1 gene are associated with dystrophic scoliosis by whole-exome sequencing. [PDF]

Front Neurol
Du Y, Bai T, Song J, Zhang L, Huang H, Han P, Gai F, Guo J, Li J, Lv C, Shao J, Zhang G, Tao H, Xi Y.   +13 more
europepmc   +1 more source

Germline mutational landscape in a large cohort of Indian breast cancer. [PDF]

BMC Cancer
Peter J, Jolly B, Raha R, Jothi J, Chakraborty A, Raman SG, Radhakrishnan S, Sivasubbu S, Scaria V, Mahalingam S.   +9 more
europepmc   +1 more source

Congenital neurodevelopmental anomalies in pediatric and young adult cancer [PDF]

, 2017
Agha, Altmann, Bailey, Baptiste, Birch, Birch, Bjorge, Bjorge, Botto, Bueno, Bursen, Carozza, Chmielecki, Ciofi, Dawson, DeBaun, Durmaz, Fisher, Gold, Good, Greenough, Hall, Harris, Hoyert, Janitz, Johnson, Johnson, Jones, Knapke, Korf, Mallol-Mesnard, Mathews, Matsumoto, McCarthy, Mili, Mili, Miller, Montes, Moore, Narod, Nishi, Partap, Rankin, Riccardi, Rice, Rios, Rosano, Samuelsen, Schmidt, Shu, Steliarova-Foucher, Sun, Sun, Sun, Vogelstein, Wilson, Windham, Witelson, Yoon, Zhang   +59 more
core   +2 more sources

Unraveling cardiac anomalies in pediatric neurofibromatosis type 1: insights and implications. [PDF]

Eur J Pediatr
Yahia S, Abdelmoneim Z, Ghozzy D, Wahba Y, Abo-Haded HM.   +4 more
europepmc   +1 more source

Laryngeal neurofibroma: case report and review of the literature. [PDF]

Front Oncol
Gao Y, Mo W, Zhu H, Zhang Y, Yang H.
europepmc   +1 more source

Beyond the Globe: Molecular Diagnostics of Optic Nerve, Orbital, and Adnexal Neoplasms. [PDF]

Transl Vis Sci Technol
Dankberg A, Yu G, Rodriguez FJ.
europepmc   +1 more source

Clinical and Genetic Characterization of Noonan Syndrome in a Romanian Cohort from Transylvania: Details on <i>PTPN11</i> c.922A>G Variant and Phenotypic Spectrum. [PDF]

Diagnostics (Basel)
Nazarie FV, Miclea D, Șufană C, Botezatu A, Popp RA, Pascanu IM, Alkhzouz C, Bucerzan S, Lazăr C, Lazea C, Vulturar R.   +10 more
europepmc   +1 more source

Recent advances in bone and soft tissue tumors: lipomatous tumors [PDF]

, 2012
Creytens, David
core   +1 more source

RENOVO-NF1 accurately predicts NF1 missense variant pathogenicity. [PDF]

Hum Genomics
Bonetti E, Pellegatta S, Rosati N, Eoli M, Mazzarella L.   +4 more
europepmc   +1 more source