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Filtros : "Fauth, Christine" Limpar

Filtros

USP affiliated authors
- kim, chong ae (~1)
- toledo, sergio pereira de almeida (~1)
Date published
- 2013 (~1)
- 2011 (~1)
Subjects
- alelopatia (1)
- carcinoma medular (1)
- cromossomos humanos (anormalidades;complicações) (1)
- doenças genéticas (diagnóstico) (1)
- fatores de crescimento (1)

Artigo de periodico
Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18 (2013)
Spreiz, Ana; Guilherme, Roberta S.; Castellan, Claudio; Green, Andrew; Rittinger, Olaf; Wellek, Brigitte; Utermann, Barbara; Erdel, Martin; Fauth, Christine; Haberlandt, Edda; Kim, Chong A.; Kulikowski, Leslie D.; Meloni, Vera A.; Utermann, Gerd; Zschocke, Johannes; Melaragno, Maria I.; Kotzot, Dieter
Source: Journal of Pediatrics. Unidade: FM
Subjects: POLIMORFISMO, DOENÇAS GENÉTICAS (DIAGNÓSTICO), ALELOPATIA, CROMOSSOMOS HUMANOS (ANORMALIDADES;COMPLICAÇÕES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SPREIZ, Ana et al. Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18. Journal of Pediatrics, v. 163, n. 4, p. 1174-1178, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.jpeds.2013.06.005. Acesso em: 01 maio 2026.
APA
Spreiz, A., Guilherme, R. S., Castellan, C., Green, A., Rittinger, O., Wellek, B., et al. (2013). Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18. Journal of Pediatrics, 163( 4), 1174-1178. doi:10.1016/j.jpeds.2013.06.005
NLM
Spreiz A, Guilherme RS, Castellan C, Green A, Rittinger O, Wellek B, Utermann B, Erdel M, Fauth C, Haberlandt E, Kim CA, Kulikowski LD, Meloni VA, Utermann G, Zschocke J, Melaragno MI, Kotzot D. Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18 [Internet]. Journal of Pediatrics. 2013 ; 163( 4): 1174-1178.[citado 2026 maio 01 ] Available from: https://doi.org/10.1016/j.jpeds.2013.06.005
Vancouver
Spreiz A, Guilherme RS, Castellan C, Green A, Rittinger O, Wellek B, Utermann B, Erdel M, Fauth C, Haberlandt E, Kim CA, Kulikowski LD, Meloni VA, Utermann G, Zschocke J, Melaragno MI, Kotzot D. Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18 [Internet]. Journal of Pediatrics. 2013 ; 163( 4): 1174-1178.[citado 2026 maio 01 ] Available from: https://doi.org/10.1016/j.jpeds.2013.06.005
Artigo de periodico
Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 (2011)
Frank-Raue, Karin; Rybicki, Lisa A.; Erlic, Zoran; Schweizer, Heiko; Winter, Aurelia; Milos, Ioana; Toledo, Sergio Pereira de Almeida; Toledo, Rodrigo A.; Tavares, Marcos R.; Alevizaki, Maria; Mian, Caterina; Siggelkow, Heide; Hüfner, Michael; Wohllk, Nelson; Opocher, Giuseppe; Dvořáková, Šárka; Bendlova, Bela; Czetwertynska, Małgorzata; Skasko, Elżbieta; Barontini, Marta; Sanso, Gabriela; Vorländer, Christian; Maia, Ana Luiza; Patocs, Attila; Links, Thera P.; de Groot, Jan Willem; Kerstens, Michiel N.; Valk, Gerlof D.; Miehle, Konstanze; Musholt, Thomas J.; Biarnes, Josefina; Damjanovic, Svetozar; Muresan, Mihaela; Wüster, Christian; Fassnacht, Martin; Peczkowska, Mariola; Fauth, Christine; Golcher, Henriette; Walter, Martin A.; Pichl, Josef; Raue, Friedhelm; Eng, Charis; Neumann, Hartmut P. H.
Source: Human mutation. Unidade: FM
Subjects: NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA), FATORES DE CRESCIMENTO, NEOPLASIAS DA TIREOIDE, GENÓTIPOS, CARCINOMA MEDULAR, FENÓTIPOS, METÁSTASE NEOPLÁSICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANK-RAUE, Karin et al. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, v. 32, n. 1, p. 51-58, 2011Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf. Acesso em: 01 maio 2026.
APA
Frank-Raue, K., Rybicki, L. A., Erlic, Z., Schweizer, H., Winter, A., Milos, I., et al. (2011). Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, 32( 1), 51-58. doi:10.1002/humu.21385
NLM
Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP de A, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, Dvořáková Š, Bendlova B, Czetwertynska M, Skasko E, Barontini M, Sanso G, Vorländer C, Maia AL, Patocs A, Links TP, de Groot JW, Kerstens MN, Valk GD, Miehle K, Musholt TJ, Biarnes J, Damjanovic S, Muresan M, Wüster C, Fassnacht M, Peczkowska M, Fauth C, Golcher H, Walter MA, Pichl J, Raue F, Eng C, Neumann HPH. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 [Internet]. Human mutation. 2011 ; 32( 1): 51-58.[citado 2026 maio 01 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf
Vancouver
Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP de A, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, Dvořáková Š, Bendlova B, Czetwertynska M, Skasko E, Barontini M, Sanso G, Vorländer C, Maia AL, Patocs A, Links TP, de Groot JW, Kerstens MN, Valk GD, Miehle K, Musholt TJ, Biarnes J, Damjanovic S, Muresan M, Wüster C, Fassnacht M, Peczkowska M, Fauth C, Golcher H, Walter MA, Pichl J, Raue F, Eng C, Neumann HPH. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 [Internet]. Human mutation. 2011 ; 32( 1): 51-58.[citado 2026 maio 01 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf

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