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Refinado por: Base de dados/Biblioteca: AUC Wiley Frozen Package in 2012 remover Base de dados/Biblioteca: Journals@Ovid remover
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11
Nell‐1, a key functional mediator of Runx2, partially rescues calvarial defects in Runx2+/− mice
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Nell‐1, a key functional mediator of Runx2, partially rescues calvarial defects in Runx2+/− mice

Zhang, Xinli ; Ting, Kang ; Bessette, Catherine M ; Culiat, Cymbeline T ; Sung, Sang Jin ; Lee, Haofu ; Chen, Feng ; Shen, Jia ; Wang, James J ; Kuroda, Shun'ichi ; Soo, Chia

Journal of bone and mineral research, 2011-04, Vol.26 (4), p.777-791 [Periódico revisado por pares]

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

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12
Cranial base abnormalities in osteogenesis imperfecta: Phenotypic and genotypic determinants
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Cranial base abnormalities in osteogenesis imperfecta: Phenotypic and genotypic determinants

Cheung, Moira S ; Arponen, Heidi ; Roughley, Peter ; Azouz, Michel E ; Glorieux, Francis H ; Waltimo‐Sirén, Janna ; Rauch, Frank

Journal of bone and mineral research, 2011-02, Vol.26 (2), p.405-413 [Periódico revisado por pares]

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

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13
Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes
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Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes

Morton, Jenny E. V. ; Frentz, Sophia ; Morgan, Tim ; Sutherland-Smith, Andrew J. ; Robertson, Stephen P.

American journal of medical genetics. Part A, 2016-10, Vol.170A (10), p.2706-2710 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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14
Extension of the mutational and clinical spectrum of SOX2 related disorders: Description of six new cases and a novel association with suprasellar teratoma
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Extension of the mutational and clinical spectrum of SOX2 related disorders: Description of six new cases and a novel association with suprasellar teratoma

Blackburn, Patrick R. ; Chacon‐Camacho, Oscar F. ; Ortiz‐González, Xilma R. ; Reyes, Mariana ; Lopez‐Uriarte, Graciela A. ; Zarei, Shabnam ; Bhoj, Elizabeth J. ; Perez‐Solorzano, Sofia ; Vaubel, Rachael A. ; Murphree, Marine I. ; Nava, Jessica ; Cortes‐Gonzalez, Vianney ; Parisi, Joseph E. ; Villanueva‐Mendoza, Cristina ; Tirado‐Torres, Iris G. ; Li, Dong ; Klee, Eric W. ; Pichurin, Pavel N. ; Zenteno, Juan C.

American journal of medical genetics. Part A, 2018-12, Vol.176 (12), p.2710-2719 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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15
Risk of ultrasound‐detected neonatal brain abnormalities in intrauterine growth‐restricted fetuses born between 28 and 34 weeks' gestation: relationship with gestational age at birth and fetal Doppler parameters
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Risk of ultrasound‐detected neonatal brain abnormalities in intrauterine growth‐restricted fetuses born between 28 and 34 weeks' gestation: relationship with gestational age at birth and fetal Doppler parameters

Cruz‐Martinez, R. ; Tenorio, V. ; Padilla, N. ; Crispi, F. ; Figueras, F. ; Gratacos, E.

Ultrasound in obstetrics & gynecology, 2015-10, Vol.46 (4), p.452-459 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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16
Masticatory loadings and cranial deformation in Macaca fascicularis: a finite element analysis sensitivity study
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Masticatory loadings and cranial deformation in Macaca fascicularis: a finite element analysis sensitivity study

Fitton, L. C. ; Shi, J. F. ; Fagan, M. J. ; O’Higgins, P.

Journal of anatomy, 2012-07, Vol.221 (1), p.55-68 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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17
Severe craniosynostosis with Noonan syndrome phenotype associated with SHOC2 mutation: Clinical evidence of crosslink between FGFR and RAS signaling pathways
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Severe craniosynostosis with Noonan syndrome phenotype associated with SHOC2 mutation: Clinical evidence of crosslink between FGFR and RAS signaling pathways

Takenouchi, Toshiki ; Sakamoto, Yoshiaki ; Miwa, Tomoru ; Torii, Chiharu ; Kosaki, Rika ; Kishi, Kazuo ; Takahashi, Takao ; Kosaki, Kenjiro

American journal of medical genetics. Part A, 2014-11, Vol.164A (11), p.2869-2872 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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18
Prenatal findings in carpenter syndrome and a novel mutation in RAB23
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Artigo
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Prenatal findings in carpenter syndrome and a novel mutation in RAB23

Haye, Damien ; Collet, Corinne ; Sembely-Taveau, Catherine ; Haddad, Georges ; Denis, Christelle ; Soulé, Nathalie ; Suc, Annie-Laure ; Listrat, Antoine ; Toutain, Annick

American journal of medical genetics. Part A, 2014-11, Vol.164A (11), p.2926-2930 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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19
Zygomatic bone shape in intentional cranial deformations: a model for the study of the interactions between skull growth and facial morphology
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Zygomatic bone shape in intentional cranial deformations: a model for the study of the interactions between skull growth and facial morphology

Ketoff, S. ; Girinon, F. ; Schlager, S. ; Friess, M. ; Schouman, T. ; Rouch, P. ; Khonsari, R. H.

Journal of anatomy, 2017-04, Vol.230 (4), p.524-531 [Periódico revisado por pares]

England: Wiley Subscription Services, Inc

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20
Impact of introduction of mid‐trimester scan on pregnancy outcome of open spina bifida in The Netherlands
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Impact of introduction of mid‐trimester scan on pregnancy outcome of open spina bifida in The Netherlands

Fleurke‐Rozema, J. H. ; Vogel, T. A. ; Voskamp, B. J. ; Pajkrt, E. ; van den Berg, P. P. ; Beekhuis, J. R. ; Bilardo, C. M. ; Brouwer, O. F. ; de Walle, H. E. K. ; Snijders, R. J. M.

Ultrasound in obstetrics & gynecology, 2014-05, Vol.43 (5), p.553-556 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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