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1Academic Journal
المؤلفون: G. Renzetti, A. Villani, C. Bizzarri, E. Vignati, A. Gianotti, M. Cappa, Juliana Szakacs, Jeanette J. Townsend, Mark E. Miller, John M. Opitz, Anne M. Kennedy, Janice L. Byrne, CHESSA, Luciana
المساهمون: G., Renzetti, A., Villani, C., Bizzarri, Chessa, Luciana, E., Vignati, A., Gianotti, M., Cappa, Juliana, Szakac, Jeanette J., Townsend, Mark E., Miller, John M., Opitz, Anne M., Kennedy, Janice L., Byrne
مصطلحات موضوعية: anterior chamber dysgenesi, aprosencephaly, atelencephaly, chromosome breakage, garcia-lurie syndrome, hydranencephaly, microphthalmia, radial dysgenesi, xk syndrome
Relation: info:eu-repo/semantics/altIdentifier/pmid/16208689; info:eu-repo/semantics/altIdentifier/wos/WOS:000232937800019; volume:138 A; issue:4; firstpage:401; lastpage:410; numberofpages:10; journal:AMERICAN JOURNAL OF MEDICAL GENETICS. PART A; http://hdl.handle.net/11573/100955; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-27444434821; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000232937800019&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a; http://www.scopus.com/inward/record.url?eid=2-s2.0-27444434821&partnerID=65&md5=f2406da5eac3918d41c34c169f6cc015
الاتاحة: http://hdl.handle.net/11573/100955
https://doi.org/10.1002/ajmg.a.30600
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000232937800019&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a
http://www.scopus.com/inward/record.url?eid=2-s2.0-27444434821&partnerID=65&md5=f2406da5eac3918d41c34c169f6cc015 -
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المؤلفون: Eugeny D. Cherstvoy, John M. Optiz, Gennady I. Lazjuk, Iosif W. Lurie, Michael K. Nedzved, Irena A. Kirillova
المصدر: American Journal of Medical Genetics. 3:303-309
مصطلحات موضوعية: business.industry, Anatomy, Aplasia, Cyclopia, medicine.disease, Alobar holoprosencephaly, Atelencephaly, Mobile cecum, Hypospadias, Aprosencephaly, medicine, XK syndrome, business, Genetics (clinical)