Results 91 to 100 of about 9,156 (193)

Multiple exostoses [PDF]

Proceedings of the Royal Society of Medicine, 1911
openaire   +2 more sources

No DNA Copy Number Changes in Osteochondromas - A Comparative Genomic Hybridization Study [PDF]

, 1997
Elomaa, Inkeri, Karaharju, Erkki, Kivioja, Aarne, Knuutila, Sakari, Larramendy, Marcelo Luis, Salmivalli, Tarja, Tarkkanen, Maija, Valle, Julio   +7 more
core   +1 more source

Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome [PDF]

, 2019
Badura-Stronka, Magdalena, Belligni, Elga, Bikker, Hennie, Bonati, Maria Teresa, Carvalho, Daniel R., Cobben, JanMaarten, Di, Donato, Nataliya, Ende, Jenneke van den, Essen, Ton van, Garavelli, Livia, Grønborg, Sabine, Haeringen, Arie van, Hagen, Johanna M. van, Hennekam, Raoul C., Herkert, Johanna C., Hollander, Nicolette S. Den, Hoogeboom, A. Jeannette M., Jamsheer, Aleksander, Latos-Bielenska, Anna, Lüdecke, Hermann-Josef, Maas, Saskia M., Maat-Kievit, Anneke, Magnani, Cinzia, Man, Stella A. de, Mannens, Marcel M., Marcelis, Carlo, Mathijssen, Inge B., Nielsen, Maartje, Otten, Ellen, Ousager, Lilian B., Pilch, Jacek, Plomp, Astrid, Poke, Gemma, Poluha, Anna, Posmyk, Renata, Rieubland, Claudine, Shaw, C. A., Silengo, Margharita, Simon, Marleen, Steen, Antony van der, Steichen, Elisabeth, Stumpel, Connie, Szakszon, Katalin, Tuin, Karin van der, Verheij, Joke B.G.M.   +44 more
core   +1 more source

Familiäre Tumorerkrankungen im Knochen [PDF]

, 2018
Zusammenfassung: Familiäre Erkrankungen, die zur Bildung von Knochentumoren führen, sind selten. Sie entwickeln sich im Zusammenhang mit genetischen Alterationen, die den Zellzyklus (Retinoblastomsyndrom/RB1, Li-Fraumeni-Syndrom/p53), wachstumssteuernde ...
Baumhoer, D., Jundt, G.
core  

Hereditary multiple exostoses. [PDF]

Journal of Medical Genetics, 1991
openaire   +3 more sources

Malignancy Ratio in Pediatric Patients with Hereditary Multiple Exostoses: True Association or Reporting Bias? [PDF]

Pediatr Rep
Comisi FF, Comisi AM, Esposito E, Savasta S.   +3 more
europepmc   +1 more source

Diagnostic familiarity with osteochondroma among primary physicians: a retrospective analysis of 195 referred cases. [PDF]

Arch Orthop Trauma Surg
Hoshi M, Aono M, Ban Y.
europepmc   +1 more source

Phenotypic Spectrum in Three Romanian Patients with 8q23-q24 Deletions. [PDF]

Int J Mol Sci
Caramizaru A, Streata I, Pirvu A, Sosoi S, Dumitrescu A, Cucu M, Camen GC, Vasile D, Braha E, Riza AL, Dobrescu A, Burada F.   +11 more
europepmc   +1 more source

Genetic Variants in DVL3 are Associated With Root Maldevelopment, Tooth Agenesis, Mesiodens, and Oral Exostoses. [PDF]

Int Dent J
Kantaputra P, Bunpiem N, Guven Y, Tripuwabhrut K, Kalayci T, Imren E, Sengtae N, Pianmee C, Pruksametanan A, Tongsima S, Ngamphiw C, Kawasaki K, Ohazama A, Cairns JRK.   +13 more
europepmc   +1 more source

Osteochondroma Arising from Dorsal Pedicle Causing Compressive Myelopathy. [PDF]

J Orthop Case Rep
Jain M, Unnava N, Sahu RN, Gupta K, Balagod R, Jayan AK.   +5 more
europepmc   +1 more source