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Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on CraniosynostosisPhenotypic integration of neurocranium and brainA genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9Fluctuating asymmetry and developmental instability in sagittal craniosynostosis.New insights into the relationship between suture closure and craniofacial dysmorphology in sagittal nonsyndromic craniosynostosis.Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosisStrengthening molecular genetics and training in craniosynostosis: The need of the hour.Syndromal and nonsyndromal primary trigonocephaly: analysis of a series of 237 patients.Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure.Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosisPrevalence and complications of single-gene and chromosomal disorders in craniosynostosis.Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.Genetic analysis of non-syndromic craniosynostosis.Laypersons' ratings of appearance in children with and without single-suture craniosynostosisCraniosynostosis: prenatal diagnosis by means of ultrasound and SSSE-MRI. Family series with report of neurodevelopmental outcome and review of the literature.Gene expression profiling in human craniosynostoses: a tool to investigate the molecular basis of suture ossification.Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications.Isolated sagittal craniosynostosis: definition, classification, and surgical indications.Congenital muscular torticollis concurrent with sagittal synostosis: a case report.Multidisciplinary care of craniosynostosisGenetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits.Perinatal features and rate of cesarean section in newborns with non-syndromic sagittal synostosis.Scalp fibroblasts have a shared expression profile in monogenic craniosynostosis.A functional aesthetic approach to correcting the sequelae of sagittal synostosis.Molecular analysis of coronal perisutural tissues in a craniosynostotic rabbit model using polymerase chain reaction suppression subtractive hybridization.A novel multidisciplinary approach toward a better understanding of cranial suture closure: the first evidence of genetic effects in adulthood.Cloning and sequencing of the rabbit FGFR2 cDNA.High-resolution imaging of craniofacial sutures: new tools for understanding the origins of craniosynostoses.Cephalic index correlates poorly with intracranial volume in non-syndromic scaphocephalic patients.Craniosynostosis : correlation with cranial vault shape and osseous defects.Genetic advances in craniosynostosis.Progressive frontal morphology changes during the first year of a modified Pi procedure for scaphocephaly.CraniosynostosisSingle suture craniosynostosis: Identification of rare variants in genes associated with syndromic formsA variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non-coding elementCraniofacial cephalometric morphology in 8-year-old children with operated sagittal synostosisCraniosynostosis, psychomotor retardation, and facial dysmorphic features in a Spanish patient with a 4q27q28.3 deletion
P2860
Q28607705-1FDDC519-93A3-4E64-ACF6-88BF146CB2F7Q28751205-E197426E-50AE-43F7-87AE-CC0446852FB0Q28943389-FFA7A89A-8239-44B0-B535-7D2A39E932ADQ33691151-A170459E-9E9C-4E76-9A6D-62984C8E1D38Q34031958-6FAC8D2A-DD09-4DF7-8427-0944F00BCF20Q34086690-EC8BCE6F-0C3F-4752-9487-C43ADD0768ABQ34236065-B80347AE-FE36-4472-8E80-29332B531FF8Q34454743-0AC05A60-20EE-49DF-8DC6-D581BCB0874BQ34472425-B3F8F17D-B487-42C5-AE71-910DB8787708Q35809894-70C7FF7D-D125-4D85-A75C-8C4B211B2275Q35988379-1DAEF8AC-E39C-4551-9721-C7BA96262518Q36504775-21AF1670-B4EA-4557-A832-250E92733967Q36629781-51EA7B68-FE78-48E1-BCD0-6FDE8B3BBAB3Q36890936-7E013998-3D4C-434C-9B9F-A9E586137570Q37134507-5391A21F-E90E-47C2-B7B2-AA817844C5B7Q37784723-4800396A-2B7C-4738-8341-FACFA2485449Q38032763-3AB6904C-B012-4DCA-9CC9-E69D4540B58AQ38032764-726BFBB5-AE8D-4F8A-AFD9-BF2D410E219AQ38032765-DF60EEEA-0E86-4623-8B76-F99E250FE078Q38266060-049110F4-635F-4C33-B1F8-2185C2C126D5Q39455637-024E65EE-C7E2-4D58-8733-B31FD269F8F7Q39993560-7770F9B3-334C-4F5A-9AFE-B3FE0038B21EQ40810247-187F6E9F-02AA-4335-AB9B-92206A8F70C4Q41554406-75B07075-17DF-4F63-A4D5-3B9A0736B8C5Q42861961-C8E3C563-8751-479C-8E26-A303A87D3E4AQ43145663-5878673B-E352-4567-BE27-5C9F1AC73CB8Q44521369-896C21AB-3AF7-42CC-8281-BE56A584B264Q48367382-5A9BE9E8-8CDF-4726-8B47-DF3A8CB6FE89Q50791497-E2BCCA6B-01C8-4358-9B01-7EF69CB26319Q51074183-7CEC9D66-944F-40FF-83F0-258CC4D885AFQ51797779-00B1382A-D4CD-4AE5-8F4C-7C902334BBF3Q52795305-9A37DF51-6F09-4C9B-ABEF-CDD32712296EQ52990661-B1D7996F-A25B-4995-A81A-BA5926FA5E8FQ56262853-476E1DAB-4676-4872-A917-214765167683Q56264797-BE4945F3-A8E4-4465-813F-A86160F841B1Q56265298-4580844F-D149-49BC-B325-208EC231D331Q56266824-7ADF32C9-3E6C-4558-AAE2-20AC58584AE0Q56266838-2CFC27EB-1BD3-44B4-BA9F-DE244E20A3F9
P2860
description
1996 nî lūn-bûn
@nan
1996 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի մարտին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Genetic study of scaphocephaly.
@ast
Genetic study of scaphocephaly.
@en
Genetic study of scaphocephaly.
@nl
type
label
Genetic study of scaphocephaly.
@ast
Genetic study of scaphocephaly.
@en
Genetic study of scaphocephaly.
@nl
prefLabel
Genetic study of scaphocephaly.
@ast
Genetic study of scaphocephaly.
@en
Genetic study of scaphocephaly.
@nl
P2093
P2860
P1476
Genetic study of scaphocephaly.
@en
P2093
Bonaïti-Pellie C
Lajeunie E
Le Merrer M
P2860
P304
P356
10.1002/(SICI)1096-8628(19960329)62:3<282::AID-AJMG15>3.0.CO;2-G
P577
1996-03-01T00:00:00Z