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Refinado por: tipo de recurso: Reports remover
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Fetus-in-fetu form of monozygotic twinning with retroperitoneal teratoma
Fetus-in-fetu form of monozygotic twinning with retroperitoneal teratoma
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Fetus-in-fetu form of monozygotic twinning with retroperitoneal teratoma

Gilbert-Barness, Enid ; Opitz, John M. ; Debich-Spicer, Diane ; Mueller, Thomas ; Arnold, Sonya R. ; Quintero, Reuben

American Journal of Medical Genetics Part A, 2003, Vol.120A (3), p.406-412

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

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2
Unusual nodular pulmonary lesions associated with thrombolytic therapy
Unusual nodular pulmonary lesions associated with thrombolytic therapy
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Unusual nodular pulmonary lesions associated with thrombolytic therapy

Carmody, Thomas James ; Wergowske, Gilbert L. ; Joffe, C. David

Catheterization and Cardiovascular Diagnosis, 1984, Vol.10 (5), p.485-488

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

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3
Netting a Corporate Web Community: Industry Sponsorship of the Internet
Netting a Corporate Web Community: Industry Sponsorship of the Internet
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Netting a Corporate Web Community: Industry Sponsorship of the Internet

Kenrich, John P ; Van Tiem, Darlene M ; Doyle, Thomas R

2001

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4
Peroneal nerve lesion after sural nerve graft harvest: An unusual complication-case report
Peroneal nerve lesion after sural nerve graft harvest: An unusual complication-case report
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Peroneal nerve lesion after sural nerve graft harvest: An unusual complication-case report

Schubert, Heinrich M. ; Wechselberger, Gottfried ; Hussl, Heribert ; Schoeller, Thomas

Microsurgery, 2005, Vol.25 (1), p.54-56

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

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5
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation
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Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation

Butler, Matthew G. ; Dagenais, Susan L. ; Garcia-Perez, José L. ; Brouillard, Pascal ; Vikkula, Miikka ; Strouse, Peter ; Innis, Jeffrey W. ; Glover, Thomas W.

American Journal of Medical Genetics Part A, 2012, Vol.158A (4), p.839-849

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

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6
Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia
Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia
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Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia

Brockmann, Knut ; Backes, Heiko ; Auber, Bernd ; Kriebel, Thomas ; Stellmer, Franziska ; Zoll, Barbara

American Journal of Medical Genetics Part A, 2009, Vol.149A (12), p.2832-2837

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

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7
Extracorporeal membrane oxygenation as a rescue of intractable ventricular fibrillation and bridge to heart transplantation
Extracorporeal membrane oxygenation as a rescue of intractable ventricular fibrillation and bridge to heart transplantation
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Extracorporeal membrane oxygenation as a rescue of intractable ventricular fibrillation and bridge to heart transplantation

Fux, Thomas ; Svenarud, Peter ; Grinnemo, Karl-Henrik ; Albåge, Anders ; Bredin, Fredrik ; van der Linden, Jan ; Hagerman, Inger ; Gabrielsen, Anders ; Lund, Lars H.

European Journal of Heart Failure, 2010, Vol.12 (3), p.301-304

Blackwell Publishing Ltd

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8
Agnathia-otocephaly complex: Report of three cases with involvement of two different Carnegie stages
Agnathia-otocephaly complex: Report of three cases with involvement of two different Carnegie stages
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Agnathia-otocephaly complex: Report of three cases with involvement of two different Carnegie stages

Schiffer, Christiane ; Tariverdian, Gholamali ; Schiesser, Monika ; Thomas, Mary C. ; Sergi, Consolato

American Journal of Medical Genetics, 2002, Vol.112 (2), p.203-208

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

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9
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation
Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation
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Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation

Seeler ; Vnencak-Jones ; Bassett ; Gilbert ; Michaelis

Haemophilia, 1999, Vol.5 (6), p.445-449

Oxford UK: Blackwell Science Ltd

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10
Summary of Radiation Research Society Online 66th Annual Meeting, Symposium on "Epidemiology: Updates on epidemiological low dose studies," including discussion
Summary of Radiation Research Society Online 66th Annual Meeting, Symposium on "Epidemiology: Updates on epidemiological low dose studies," including discussion
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Summary of Radiation Research Society Online 66th Annual Meeting, Symposium on "Epidemiology: Updates on epidemiological low dose studies," including discussion

Milder, Cato M. ; Kendall, Gerald M. ; Arsham, Aryana ; Schöllnberger, Helmut ; Wakeford, Richard ; Cullings, Harry M. ; Little, Mark P.

International Journal of Radiation Biology: The Second Bill Morgan Memorial Special Issue: An update on low dose biology, epidemiology, its integration and implications for radiation protection, 2021, Vol.97 (6), p.866-873

Taylor & Francis

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