A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family
about
PLEXIN-D1, a novel plexin family member, is expressed in vascular endothelium and the central nervous system during mouse embryogenesisHOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- miceCongenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements.Congenital innervation dysgenesis syndrome (CID)/congenital cranial dysinnervation disorders (CCDDs)The genetics of strabismusDe novo mutations in PLXND1 and REV3L cause Möbius syndromeRecent progress in understanding congenital cranial dysinnervation disordersOrthopedic Manifestations of Mobius Syndrome: Case Series and Survey StudyMoebius sequence -a multidisciplinary clinical approach.Vascular endothelial growth factor controls neuronal migration and cooperates with Sema3A to pattern distinct compartments of the facial nerve.An exome sequencing study of Moebius syndrome including atypical cases reveals an individual with CFEOM3A and a TUBB3 mutation.Examining the genetics of congenital facial paralysis--a closer look at Moebius syndrome.Congenital cranial dysinnervation disorders.A Novel Loss-of-Function Mutation in HOXB1 Associated with Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family.Living with Moebius syndrome: adjustment, social competence, and satisfaction with life.Wilms' tumor in a case with Möbius' syndrome associated with arthrogryposis and mega cisterna magna.
P2860
Q28212775-46554D2A-814D-4867-B864-0974CF33117FQ30459147-4608D2C8-B806-41B9-A81D-3227D6A0EA43Q34123574-880DF574-4E34-4E88-AC05-F0D98DE9710DQ35359083-84F2DA50-B2C5-4DD1-BECB-BBD4100236B6Q35876992-089E2F4B-6A6A-4F50-A0C5-5BEB67B03516Q36287506-084DD283-8E33-49CE-A79A-FDDF4B6941CEQ36474129-1CA75C9D-3E4C-40F4-AF1B-2D794BD1B60AQ36601515-C626473B-1561-4D5B-A0D1-D4E97E425156Q37566061-F67F03FE-B81B-4D1E-B5E0-B7ADE000194CQ37621018-1F48AA39-D7F2-4B6F-9DC0-9B0F1486BEDBQ37678113-1C1D2FDF-E87A-4E72-A042-9E9CC92D7AC6Q38348660-40922492-21E6-4826-9422-E28848A4C0D7Q39006051-7EF081E4-93DA-4F56-8621-163A0DC6BF8CQ49637757-6CFB23C3-C4E1-4C41-8985-83E54131B030Q50703731-752C12A0-7AAF-46BC-A9C9-253A1C46075DQ52091795-873100BF-2209-4F66-888D-CDF53511C233
P2860
A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family
description
1999 nî lūn-bûn
@nan
1999 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
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1999年学术文章
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1999年学术文章
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1999年学术文章
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1999年学术文章
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1999年学术文章
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1999年學術文章
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name
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@ast
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@en
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@nl
type
label
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@ast
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@en
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@nl
prefLabel
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@ast
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@en
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@nl
P2093
P2860
P356
P1476
A second gene for autosomal do ...... omosome 10q, in a Dutch family
@en
P2093
Padberg GW
Verzijl HT
van den Helm B
P2860
P304
P356
10.1086/302539
P407
P577
1999-09-01T00:00:00Z