खोज परिणाम - Ethylin Wang Jabs

परिणाम को परिष्कृत करें
  1. 1
    Genetic basis of potential therapeutic strategies for craniosynostosis

    Genetic basis of potential therapeutic strategies for craniosynostosis द्वारा Heather Melville, Yingli Wang, Peter J. Taub, Ethylin Wang Jabs

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें
    Revisão
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    में बचाया:
  2. 2
    Characterization of an alpha 1—-3-galactosyltransferase homologue on human chromosome 12 that is organized as a processed pseudogene.

    Characterization of an alpha 1—-3-galactosyltransferase homologue on human chromosome 12 that is organized as a processed pseudogene. द्वारा David H. Joziasse, J H Shaper, Ethylin Wang Jabs, Nancy L. Shaper

    प्रकाशित 1991
    पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  3. 3
    Parental origin of mutations in sporadic cases of Treacher Collins syndrome

    Parental origin of mutations in sporadic cases of Treacher Collins syndrome द्वारा Alessandra Splendore, Ethylin Wang Jabs, Têmis Maria Félix, Maria Rita Passos‐Bueno

    प्रकाशित 2003
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    Artigo
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    में बचाया:
  4. 4
    Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses

    Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses द्वारा Yann Heuzé, G.H. Holmes, Inga Peter, Joan T. Richtsmeier, Ethylin Wang Jabs

    प्रकाशित 2014
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    Artigo
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    में बचाया:
  5. 5
    The human aquaporin-CHIP gene. Structure, organization, and chromosomal localization

    The human aquaporin-CHIP gene. Structure, organization, and chromosomal localization द्वारा Chulso Moon, Gregory M. Preston, C.A. Griffin, Ethylin Wang Jabs, Peter Agre

    प्रकाशित 1993
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    Artigo
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    में बचाया:
  6. 6
    FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models

    FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models द्वारा Neus Martínez‐Abadías, Yann Heuzé, Yingli Wang, Ethylin Wang Jabs, Kristina Aldridge, Joan T. Richtsmeier

    प्रकाशित 2011
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    Artigo
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    में बचाया:
  7. 7
    Ten-year experience of more than 35,000 orofacial clefts in Africa

    Ten-year experience of more than 35,000 orofacial clefts in Africa द्वारा Julia C Conway, Peter J. Taub, Rochelle Kling, Kurun Oberoi, John Doucette, Ethylin Wang Jabs

    प्रकाशित 2015
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    Artigo
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    में बचाया:
  8. 8
    Oculodentodigital dysplasia connexin43 mutations result in non-functional connexin hemichannels and gap junctions in C6 glioma cells

    Oculodentodigital dysplasia connexin43 mutations result in non-functional connexin hemichannels and gap junctions in C6 glioma cells द्वारा Albert Lai, Dung-Nghi Le, William A. Paznekas, Wes D. Gifford, Ethylin Wang Jabs, Andrew Charles

    प्रकाशित 2006
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    Artigo
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    में बचाया:
  9. 9
    Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public

    Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public द्वारा Saskia C. Sanderson, Sabrina A. Suckiel, Micol Zweig, Erwin P. Böttinger, Ethylin Wang Jabs, Lynne D. Richardson

    प्रकाशित 2015
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  10. 10
    Mapping the Treacher Collins syndrome locus to 5q31.3→q33.3

    Mapping the Treacher Collins syndrome locus to 5q31.3→q33.3 द्वारा Ethylin Wang Jabs, Xiang Li, Cathleen A. Coss, Eugene W. Taylor, Deborah A. Meyers, James L. Weber

    प्रकाशित 1991
    पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  11. 11
    The Paternal-Age Effect in Apert Syndrome Is Due, in Part, to the Increased Frequency of Mutations in Sperm

    The Paternal-Age Effect in Apert Syndrome Is Due, in Part, to the Increased Frequency of Mutations in Sperm द्वारा Rivka L. Glaser, Karl W. Broman, Rebecca L. Schulman, Brenda Eskenazi, Andrew J. Wyrobek, Ethylin Wang Jabs

    प्रकाशित 2003
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  12. 12
    Functional Characterization of Connexin43 Mutations Found in Patients With Oculodentodigital Dysplasia

    Functional Characterization of Connexin43 Mutations Found in Patients With Oculodentodigital Dysplasia द्वारा Junko Shibayama, William A. Paznekas, Akiko Seki, Steven M. Taffet, Ethylin Wang Jabs, Mario Delmar, Hassan Musa

    प्रकाशित 2005
    पूर्ण पाठ प्राप्त करें
    Artigo
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  13. 13
    Tissue‐specific responses to aberrant FGF signaling in complex head phenotypes

    Tissue‐specific responses to aberrant FGF signaling in complex head phenotypes द्वारा Neus Martínez‐Abadías, Susan M. Motch, Talia L. Pankratz, Yingli Wang, Kristina Aldridge, Ethylin Wang Jabs, Joan T. Richtsmeier

    प्रकाशित 2012
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    Artigo
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    में बचाया:
  14. 14
    Clinical spectrum of fibroblast growth factor receptor mutations

    Clinical spectrum of fibroblast growth factor receptor mutations द्वारा M.R. Passos-Bueno, W.R. Wilcox, Ethylin Wang Jabs, Andréa L. Sertié, Luís Garcia Alonso, H. Kitoh

    प्रकाशित 1999
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    Artigo
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    में बचाया:
  15. 15
    Clinical spectrum of fibroblast growth factor receptor mutations

    Clinical spectrum of fibroblast growth factor receptor mutations द्वारा Maria Rita Passos‐Bueno, William R. Wilcox, Ethylin Wang Jabs, Andr�a L. Serti�, Luís Garcia Alonso, Hiroshi Kitoh

    प्रकाशित 1999
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    Artigo
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    में बचाया:
  16. 16
    Characterization of the Nucleolar Gene Product, Treacle, in Treacher Collins Syndrome

    Characterization of the Nucleolar Gene Product, Treacle, in Treacher Collins Syndrome द्वारा Cynthia Isaac, Karen L. Marsh, William A. Paznekas, Jill Dixon, Michael J. Dixon, Ethylin Wang Jabs, U. Thomas Meier

    प्रकाशित 2000
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    Artigo
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    में बचाया:
  17. 17
    Associations between periconceptional alcohol consumption and craniosynostosis, omphalocele, and gastroschisis

    Associations between periconceptional alcohol consumption and craniosynostosis, omphalocele, and gastroschisis द्वारा Sandra D. Richardson, Marilyn L. Browne, Sonja A. Rasmussen, Charlotte M. Druschel, Lixian Sun, Ethylin Wang Jabs, Paul A. Romitti

    प्रकाशित 2011
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    Artigo
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    में बचाया:
  18. 18
    The Ups and Downs of Mutation Frequencies during Aging Can Account for the Apert Syndrome Paternal Age Effect

    The Ups and Downs of Mutation Frequencies during Aging Can Account for the Apert Syndrome Paternal Age Effect द्वारा Song-Ro Yoon, Jian Qin, Rivka L. Glaser, Ethylin Wang Jabs, Nancy S. Wexler, Rebecca Z. Sokol, Norman Arnheim, Peter Calabrese

    प्रकाशित 2009
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    Artigo
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    में बचाया:
  19. 19
    <i>TCOF1</i> gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region

    <i>TCOF1</i> gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region द्वारा Carol A. Wise, Lydia C. Chiang, William A. Paznekas, Mridula Sharma, Maurice M. Musy, Jennifer Ashley, Michael Lovett, Ethylin Wang Jabs

    प्रकाशित 1997
    पूर्ण पाठ प्राप्त करें
    Artigo
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  20. 20
    Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm

    Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm द्वारा Andrew J. Wyrobek, Brenda Eskenazi, Suzanne Young, Norman Arnheim, Irene Tiemann‐Boege, Ethylin Wang Jabs, Rivka L. Glaser, Francesca Pearson, D.P. Evenson

    प्रकाशित 2006
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    Artigo
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