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Documents 1-6 out of 6 found
  Current Search:  oral: 25196, facial: 137, digit: 2850, syndrom: 4037, 1: 484355, pseudogen: 330, 2: 313487  

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Bibliography for H-22845
PubMed · H-22845 "ED2-positive perivascular phagocytes produce interleukin-1beta during delayed neuronal loss in the facial nucleus of the rat." Angelov DN, Walther M, Streppel M, Guntinas-Lichius O, van Dam AM, Stennert E, Neiss WF.
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Bibliography for D-8998
PubMed · D-1956 · D-8998 "Trigeminal projections to hypoglossal and facial motor nuclei in the rat." Pinganaud G, Bernat I, Buisseret P, Buisseret-Delmas C.
PubMed · D-1817 · D-8998 "Reinnervation by axon collaterals from single facial motoneurons to multiple muscle targets following axotomy in the adult guinea pig." Ito M, Kudo M.

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PT3699-3E (PR27547) Hu Plas 12K page 318
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author: emmachleder updated: 22/08/2002 matching: oral facial digit syndrom 1 2
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Kinase-Disease Associations
RSK2 (RPS6KA3) AGC CNS, Development, Virology LOF Mut LOF mutations cause dominant Coffin-Lowry syndrome [OMIM:303600] characterized by severe mental retardation with facial, digital and progressive skeletal deformations.
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Bibliography for N-21485
PubMed · N-21485 "Non-overlapping thalamocortical projections for separate forepaw digits before and after cortical reorganization in the raccoon." Rasmusson DD, Nance DM.
PubMed · N-21485 "Representation of whisker follicle intrinsic musculature in the facial motor nucleus of the rat." Klein BG, Rhoades RW.

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- The Jackson Laboratory
Split hand/split foot, syndactyly, urinary tract obstruction, radial, diaphragmatic, and neural tube defects: Czeizel-Losonci syndrome?.
A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parents.

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