A-2 Cerabral abnormalities in the homozygous legless mouse (lgl/lgl).
スポンサーリンク
概要
著者
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Naruse I.
School of Health Science, Faculty of Medicine, Tottori University
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Bell S.
Children's Hospital Research Foundation University Of Cincinnati
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SCHREINER C.
Children's Hospital Research Foundation, University of Cincinnati
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SCOTT W.
Children's Hospital Research Foundation, University of Cincinnati
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Schreiner C.
Children's Hospital Research Foundation University Of Cincinnati
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Naruse I.
School Of Health Science Faculty Of Medicine Tottori University
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Scott W.
Children's Hospital Research Foundation University Of Cincinnati
関連論文
- Integration of a transposon into Gil3 in the genetic polydactyly/arhinencephaly mouse(Pdn/Pdn)(Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
- Over-expression of the Shh gene in the genetic polydactyly/arhinencephaly mouse (Pdn/Pdn) in which the gene responsible is Gil3(Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
- O-58 Analysis of Gli3 and Shh gene expressions in the genetic polydactyly/arhinencephaly mouse,(Pdn/Pdn)
- A-2 Cerabral abnormalities in the homozygous legless mouse (lgl/lgl).
- Exencephaly and embryonic lethality in Cbp knockout mouse embryo
- B-09 Phenotypic Similarity in Rubinstein-Taybi Syndrome and Knockout Mice in Cbp Gene.
- O-59 Hydrocephalus manifestation in the genetic polydactyly/arhinencephaly mouse (Pdn/Pdn)
- S2-2 Mechanism of polydactyly menifestation in mice and its extrapolation to human. (II. Limb Malformations : Mechanism, Diagnosis, and Therapy)