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2-Hour Accelerated Diagnostic Protocol to Assess Patients With Chest Pain Symptoms Using Contemporary Troponins as the Only Biomarker: The ADAPT Trial
2-Hour Accelerated Diagnostic Protocol to Assess Patients With Chest Pain Symptoms Using Contemporary Troponins as the Only Biomarker: The ADAPT Trial
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2-Hour Accelerated Diagnostic Protocol to Assess Patients With Chest Pain Symptoms Using Contemporary Troponins as the Only Biomarker: The ADAPT Trial

THAN, Martin ; CULLEN, Louise ; TROUGHTON, Richard ; BROWN, Anthony F. T ; GEORGE, Peter ; FLORKOWSKI, Christopher M ; KLINE, Jeffrey A ; FRANK PEACOCK, W ; MAISEL, Alan S ; SWEE HAN LIM ; LAMANN, Arvin ; MARK RICHARDS, A ; ALDOUS, Sally ; PARSONAGE, William A ; REID, Christopher M ; GREENSLADE, Jaimi ; FLAWS, Dylan ; HAMMETT, Christopher J ; BEAM, Daren M ; ARDAGH, Michael W

Journal of the American College of Cardiology, 2012-06, Vol.59 (23), p.2091-2098 [Periódico revisado por pares]

New York, NY: Elsevier

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2
22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in Brazil
22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in Brazil
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22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in Brazil

Rosa, Rafael F.M. ; Pilla, Carlo B. ; Pereira, Vera L.B. ; Flores, José A.M. ; Golendziner, Eliete ; Koshiyama, Dayane B. ; Hertz, Michele T. ; Ricachinevsky, Cláudia P. ; Roman, Tatiana ; Varella-Garcia, Marileila ; Paskulin, Giorgio A.

American journal of medical genetics. Part A, 2008-07, Vol.146A (13), p.1655-1661 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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3
47,XXX male: A clinical and molecular study
47,XXX male: A clinical and molecular study
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47,XXX male: A clinical and molecular study

Ogata, Tsutomu ; Matsuo, Mari ; Muroya, Koji ; Koyama, Yasuhiro ; Fukutani, Keiko

American journal of medical genetics, 2001-02, Vol.98 (4), p.353-356 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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4
48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome
48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome
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48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome

Tartaglia, Nicole ; Ayari, Natalie ; Howell, Susan ; D'Epagnier, Cheryl ; Zeitler, Philip

Acta Paediatrica, 2011-06, Vol.100 (6), p.851-860 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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5
49, XXXXY Syndrome with Unilateral Renal Aplasia, Proteinuria, and Venous Thromboembolism
49, XXXXY Syndrome with Unilateral Renal Aplasia, Proteinuria, and Venous Thromboembolism
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49, XXXXY Syndrome with Unilateral Renal Aplasia, Proteinuria, and Venous Thromboembolism

OKUYAMA, Shin ; WAKUI, Hideki ; KANEKO, Junji ; MASAI, Rie ; OHTANI, Hiroshi ; KOMATSUDA, Atsushi ; SAWADA, Ken-ichi

Internal Medicine, 2004, Vol.43(12), pp.1186-1190 [Periódico revisado por pares]

Tokyo: The Japanese Society of Internal Medicine

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6
A 3q+ marker chromosome in EBV‐carrying nasopharyngeal carcinomas
A 3q+ marker chromosome in EBV‐carrying nasopharyngeal carcinomas
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A 3q+ marker chromosome in EBV‐carrying nasopharyngeal carcinomas

Mitelman, F. ; Mark‐Vendel, E. ; Mineur, A. ; Giovanella, B. ; Klein, G.

International journal of cancer, 1983-12, Vol.32 (6), p.651-655 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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7
Abdominal Burkitt-type lymphomas in Algeria
Abdominal Burkitt-type lymphomas in Algeria
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Abdominal Burkitt-type lymphomas in Algeria

LADJADJ, Y ; PHILIP, T ; LENOIR, G. M ; TAZEROUT, F. Z ; BENDISARI, K ; BOUKHELOUA, R ; BIRON, P ; BRUNAT-MENTIGNY, M ; ABOULOLA, M

British journal of cancer, 1984-04, Vol.49 (4), p.503-512 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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8
Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes
Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes
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Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes

Taibjee, S.M. ; Bennett, D.C. ; Moss, C.

British journal of dermatology (1951), 2004-08, Vol.151 (2), p.269-282 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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9
Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia
Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia
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Abnormal telomere metabolism in Fanconi's anaemia correlates with genomic instability and the probability of developing severe aplastic anaemia

Li, Xiaxin ; Leteurtre, François ; Rocha, Vanderson ; Guardiola, Philippe ; Berger, Roland ; Daniel, Marie‐Therese ; Noguera, Maria Helena ; Maarek, Odile ; Roux, Gwenaëlle L. E. ; De La Salmonière, Pauline ; Richard, Patrice ; Gluckman, Eliane

British journal of haematology, 2003-03, Vol.120 (5), p.836-845 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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10
Abnormalities of the umbilico‐portal venous system in Down syndrome: A report of two new patients
Abnormalities of the umbilico‐portal venous system in Down syndrome: A report of two new patients
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Abnormalities of the umbilico‐portal venous system in Down syndrome: A report of two new patients

Pipitone, Salvatore ; Garofalo, Caterina ; Corsello, Giovanni ; Mongiovì, Maurizio ; Piccione, Maria ; Maresi, Emiliano ; Sperandeo, Velio

American journal of medical genetics, 2003-08, Vol.120A (4), p.528-532 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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