about
Genetic Syndromes Associated with CraniosynostosisFibroblast growth factor receptor signaling in hereditary and neoplastic disease: biologic and clinical implicationsQuantification of facial skeletal shape variation in fibroblast growth factor receptor-related craniosynostosis syndromes.A case of Pfeiffer syndrome with c833_834GC>TG (Cys278Leu) mutation in the FGFR2 gene.Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.Molecular Analysis of Twist1 and FGF Receptors in a Rabbit Model of Craniosynostosis: Likely Exclusion as the Loci of OriginSpatial and Temporal Analysis of Active ERK in the C. elegans Germline.Craniosynostosis genetics: The mystery unfolds.Craniosynostosis: imaging review and primer on computed tomography.Unique airway finding in a case of Pfeiffer syndrome and its management.Apert syndrome: report of a case with emphasis on oral manifestations.Selective mutation accumulation: a computational model of the paternal age effect.Pfeiffer syndrome.Molecular analysis of coronal perisutural tissues in a craniosynostotic rabbit model using polymerase chain reaction suppression subtractive hybridization.Cloning of TgfβR1 and TgfβR2 and Likely Exclusion as Loci of Origin in a Rabbit Craniosynostotic Model.Novel chromosomal microduplications associated with dolichocephaly craniosynostosis: A case report.Ontogeny of the spheno-occipital synchondrosis in a modern Queensland, Australian population using computed tomography.Pfeiffer syndrome: oral healthcare management and description of new dental findings in a craniosynostosis.Clinical expression in Pfeiffer syndrome type 2 and 3: surveillance in Japan.Intestinal malrotation in a patient with Pfeiffer syndrome type 2.A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndromeBiallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromesRadiographic manifestations in Pfeiffer syndromeA rare case of Pfeiffer's syndrome
P2860
Q26745874-253CDA56-7C6E-454F-A284-260CC57C94ADQ26801718-D4F43BB8-6DF2-4EA0-B502-99E1BFF64547Q33642091-4BC6EEC7-2847-407F-A8CF-4DA8C6578DFBQ34417370-DFF448F2-1F97-47C7-BBBC-6EC06AC66FA0Q35059805-FE60A995-E2B3-4575-8646-D4264214E7FDQ36877141-7850A291-5439-4009-9115-901F9C89FEE1Q37580008-B060CDE2-2319-4DA0-9A97-F783309AAF2CQ37957083-DA8D0A95-16DA-492A-986F-1B6DDED0EB53Q38103453-EEBE9DBC-CE4B-45BB-9E90-3AFC5E3A9378Q38259929-A6955E35-2A9F-4ABE-843E-58EC017B9793Q38606156-435F5DBB-1B84-40DB-B7C2-2D3BA07CEDAEQ39484217-ADD9E287-3DE5-490A-9872-0B7749E7F9E8Q40116942-458E97D3-BA14-4631-BEB5-FDAB2930A175Q43145663-D6D8FC75-490E-4129-A487-BE34B1690981Q44850022-BC202681-9EA1-4F4B-BACA-057603478101Q47161866-567BD55F-7550-47E7-A5F7-BF6DBE6DC0B0Q47449139-285AAE7A-8C4F-45B1-9EB0-7C49C4667B72Q53094512-77A40BC2-3736-4D49-AC60-C590CA0C0793Q54484909-E87363FD-6888-485C-A319-07CEE6106C54Q54671535-BC37C842-8625-4614-A700-56A4CB5F5DCAQ56265502-A18689E3-68F8-4FD9-84EA-E5421843A85FQ56266483-A411C564-2E9F-4F64-A207-A6AABAB7FAD1Q56266802-E4ECBF55-FB49-4AAB-A5FC-9FA6BCA801D3Q56333086-3ADC7469-2314-4864-875C-6D2E0EB9E613
P2860
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Pfeiffer syndrome
@ast
Pfeiffer syndrome
@en
Pfeiffer syndrome
@en-gb
Pfeiffer syndrome
@nl
type
label
Pfeiffer syndrome
@ast
Pfeiffer syndrome
@en
Pfeiffer syndrome
@en-gb
Pfeiffer syndrome
@nl
prefLabel
Pfeiffer syndrome
@ast
Pfeiffer syndrome
@en
Pfeiffer syndrome
@en-gb
Pfeiffer syndrome
@nl
P2860
P3181
P356
P1476
Pfeiffer syndrome
@en
P2093
Annick Vogels
P2860
P2888
P3181
P356
10.1186/1750-1172-1-19
P407
P5008
P577
2006-06-01T00:00:00Z
P5875
P6179
1020746872