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1
Identification and Evaluation of Items for Vitreoretinal Diseases Quality of Life Item Banks.
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A Neuropsychological Profile for Cerebrotendinous Xanthomatosis: A Single-Case Study.
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Recommended Treatment for Antibody-mediated Rejection After Kidney Transplantation: the 2019 Expert Consensus From the Transplant Society Working Group.
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TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.
Bakhuizen, J J;Hogervorst, F B;Velthuizen, M E;Ruijs, M W;van Engelen, K;van Os, T A;Gille, J J;Coll...
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osler-weber-rendu syndrome: a case report with familial clustering
;Grover Sanjiv;Grewal R;Verma Rajesh;Sahni H;Muralidhar R;Sinha Preema
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dubin-johnson syndrome. (a case report and review of literature).
;Barve J;Kelkar S;Chikhalikar A;Pimparkar B
1982 international islamic university malaysia engineer... 202 views
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from families syndromes to genes… the first clinical and genetic characterizations of hereditary syndromes predisposing to cancer: what was the beginning?
;Charité Ricker, MS, LCGC
2017 hla DOI: 10.1016/j.rmclc.2017... 159 views
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medical image of the week: bronchial clot removal via cryotherapy
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9
Hereditary Diffuse Gastric Cancer: Prophylactic Surgical Oncology Implications
Henry T. Lynch,Edibaldo Silva,Debrah Wirtzfeld,Pamela Hebbard,Jane Lynch,David G. Huntsman;Henry T....
2008 surgical clinics of north america DOI: 10.1016/j.suc.2008.0... 140 views
10
Genomic landscape of colorectal carcinogenesis.
Kim, Jin Cheon;Bodmer, Walter F;
2022 Journal of cancer research and clinical oncology DOI: 10.1007/s00432-021-0... 142 views
11
A tuber mustard AP2/ERF transcription factor gene, , functioning in abscisic acid and abiotic stress responses, and evolutionary trajectory of the homologous genes in species.
Xiang, Liuxin;Liu, Chao;Luo, Jingzhi;He, Lin;Deng, Yushan;Yuan, Jie;Wu, Chaofeng;Cai, Yingfan;
2018 PeerJ DOI: 10.7717/peerj.6071 411 views
12
Frequency of CDH1 germline variants and contribution of dietary habits in early age onset gastric cancer patients in Brazil.
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2019 gastric cancer : official journal of the internati... DOI: 10.1007/s10120-019-0... 327 views
13
The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3.
Nicholson, G A;Dawkins, J L;Blair, I P;Kennerson, M L;Gordon, M J;Cherryson, A K;Nash, J;Bananis, T;
1996 nature genetics 218 views
14
New germline BRCA2 gene variant in the Tuvinian Mongol breast cancer patients.
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15
Maternal folic acid depletion during early pregnancy increases sensitivity to squamous tumor formation in the offspring in mice.
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16
Hepatocellular carcinoma: epidemiology and risk factors
Michael C Kew and
2014 journal of hepatocellular carcinoma DOI: 10.2147/JHC.S44381 173 views
17
Novel Deleterious nsSNPs within MEFV Gene that Could Be Used as Diagnostic Markers to Predict Hereditary Familial Mediterranean Fever: Using Bioinformatics Analysis
Mustafa, Mujahed I.;Abdelhameed, Tebyan A.;Abdelrhman, Fatima A.;Osman, Soada A.;Hassan, Mohamed A.;...
2019 advances in bioinformatics DOI: 10.1155/2019/1651587 647 views
18
Comorbidity of Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Disease Exert Significant Effect on RBC Indices
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2019 anemia DOI: 10.1155/2019/3179173 271 views
19
Identification and Mapping of a 2,009-bp DNA Deletion in SERPING1 of a Hereditary Angioedema Patient
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2019 case reports in genetics DOI: 10.1155/2019/7052062 210 views
20
Flow Cytometric Test with Eosin-5-Maleimide for a Diagnosis of Hereditary Spherocytosis in a Newborn
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2019 case reports in hematology DOI: 10.1155/2019/5925731 163 views

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quality of life retina retinal disease computerised adaptive testing item banks patient-reported outcome instruments vitreoretinal diseases dementia differential diagnosis congenital cerebrotendinous xanthomatosis and neonatal disease and abnormalities cerebellar ataxia genetic disease Breast cancer genetic testing tp53 li–fraumeni syndrome adult diagnosis