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Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests
Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests
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Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests

Pujol, P. ; Lyonnet, D. Stoppa ; Frebourg, T. ; Blin, J. ; Picot, M. C. ; Lasset, C. ; Dugast, C. ; Berthet, P. ; de Paillerets, B. Bressac ; Sobol, H. ; Grandjouan, S. ; Soubrier, F. ; Buecher, B. ; Guimbaud, R. ; Lidereau, R. ; Jonveaux, P. ; Houdayer, C. ; Giraud, S. ; Olschwang, S. ; Nogue, E. ; Galibert, V. ; Bara, C. ; Nowak, F. ; Khayat, D. ; Nogues, C.

Breast cancer research and treatment, 2013-08, Vol.141 (1), p.135-144 [Periódico revisado por pares]

Boston: Springer US

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2
Diagnosis of patients with Lynch syndrome lacking the Amsterdam II or Bethesda criteria
Diagnosis of patients with Lynch syndrome lacking the Amsterdam II or Bethesda criteria
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Diagnosis of patients with Lynch syndrome lacking the Amsterdam II or Bethesda criteria

Trujillo-Rojas, Miguel Angel ; Ayala-Madrigal, María de la Luz ; Gutiérrez-Angulo, Melva ; González-Mercado, Anahí ; Moreno-Ortiz, José Miguel

Hereditary cancer in clinical practice, 2023-10, Vol.21 (1), p.1-21, Article 21 [Periódico revisado por pares]

London: BioMed Central Ltd

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3
Correction: Genome-wide identification and expression characterization of the DoG gene family of moso bamboo (Phyllostachys edulis)
Correction: Genome-wide identification and expression characterization of the DoG gene family of moso bamboo (Phyllostachys edulis)
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Correction: Genome-wide identification and expression characterization of the DoG gene family of moso bamboo (Phyllostachys edulis)

Zhijun, Zhang ; Peiyao, Yu ; Bing, Huang ; Ruifang, Ma ; Vinod, Kunnummal Kurungara ; Ramakrishnan, Muthusamy

BMC genomics, 2023-03, Vol.24 (1), p.128-128, Article 128 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
Target-allele-specific probe single-base extension
Target-allele-specific probe single-base extension
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Target-allele-specific probe single-base extension

Chen, Qiong ; Yang, Xuexi ; Huang, Weilun ; Li, Ziyan ; Xu, Mingli ; Li, Yang ; Tao, Fangchao

Human genetics, 2023-03, Vol.142 (3), p.445 [Periódico revisado por pares]

Springer

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5
Target-allele-specific probe single-base extension : a novel MALDI-TOF-MS strategy for multi-variants analysis and its application in simultaneous detection of [alpha]-/[beta]-thalassemia mutations
Target-allele-specific probe single-base extension : a novel MALDI-TOF-MS strategy for multi-variants analysis and its application in simultaneous detection of [alpha]-/[beta]-thalassemia mutations
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Target-allele-specific probe single-base extension : a novel MALDI-TOF-MS strategy for multi-variants analysis and its application in simultaneous detection of [alpha]-/[beta]-thalassemia mutations

Chen, Qiong ; Yang, Xuexi ; Huang, Weilun ; Li, Ziyan ; Xu, Mingli ; Li, Yang ; Tao, Fangchao

Human genetics, 2023-03, Vol.142 (3), p.445 [Periódico revisado por pares]

Springer

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6
Correction: Myocardial native T1 mapping and extracellular volume quantification in asymptomatic female carriers of Duchenne muscular dystrophy gene mutations
Correction: Myocardial native T1 mapping and extracellular volume quantification in asymptomatic female carriers of Duchenne muscular dystrophy gene mutations
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Correction: Myocardial native T1 mapping and extracellular volume quantification in asymptomatic female carriers of Duchenne muscular dystrophy gene mutations

Masárová, Lucia ; Panovský, Roman ; PeÅ¡l, Martin ; Mary, Luz Mojica-Pisciotti ; Holecek, TomáÅ ; Kincl, Vladimír ; JuÅíková, Lenka ; Máchal, Jan ; OpatÅil, LukáÅ ; Feitová, VÄra

Orphanet journal of rare diseases, 2023-10, Vol.18 (1), p.1-331, Article 331 [Periódico revisado por pares]

London: BioMed Central Ltd

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7
Detecting haplotype-specific transcript variation in long reads with FLAIR2
Detecting haplotype-specific transcript variation in long reads with FLAIR2
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Detecting haplotype-specific transcript variation in long reads with FLAIR2

Tang, Alison D. ; Felton, Colette ; Hrabeta-Robinson, Eva ; Volden, Roger ; Vollmers, Christopher ; Brooks, Angela N.

Genome Biology, 2024-07, Vol.25 (1), p.173, Article 173 [Periódico revisado por pares]

London: BioMed Central

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8
Correction: The LEA gene family in tomato and its wild relatives: genome-wide identifcation, structural characterization, expression profling, and role of SlLEA6 in drought stress
Correction: The LEA gene family in tomato and its wild relatives: genome-wide identifcation, structural characterization, expression profling, and role of SlLEA6 in drought stress
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Correction: The LEA gene family in tomato and its wild relatives: genome-wide identifcation, structural characterization, expression profling, and role of SlLEA6 in drought stress

Jia, Chunping ; Guo, Bin ; Wang, Baike ; Li, Xin ; Yang, Tao ; Li, Ning ; Wang, Juan ; Yu, Qinghui

BMC plant biology, 2023-01, Vol.23 (1), p.57-57, Article 57 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
Correction to: CC16 polymorphisms in asthma, asthma subtypes, and asthma control in adults from the Agricultural Lung Health Study
Correction to: CC16 polymorphisms in asthma, asthma subtypes, and asthma control in adults from the Agricultural Lung Health Study
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Correction to: CC16 polymorphisms in asthma, asthma subtypes, and asthma control in adults from the Agricultural Lung Health Study

Gribben, K C ; Wyss, A B ; Poole, J A ; Farazi, P A ; Wichman, C ; Richards-Barber, M ; Freeman, L E Beane ; Henneberger, P K ; Umbach, D M ; London, S J ; LeVan, T D

Respiratory research, 2022-12, Vol.23 (1), p.350-350, Article 350 [Periódico revisado por pares]

England: BioMed Central Ltd

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10
Correction: TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2
Correction: TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2
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Correction: TP63 truncating mutation causes increased cell apoptosis and premature ovarian insufficiency by enhanced transcriptional activation of CLCA2

Fan, Yali ; Chen, Shuya ; Chu, Chunfang ; Yin, Xiaodan ; Jin, Jing ; Zhang, Lingyan ; Yan, Huihui ; Cao, Zheng ; Liu, Ruixia ; Xin, Mingwei ; Li, Lin ; Yin, Chenghong

Journal of ovarian research, 2024-04, Vol.17 (1), p.93-93, Article 93 [Periódico revisado por pares]

England: BioMed Central Ltd

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