About: Clinical Dysmorphology

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Attributes	Values
rdf:type	Item
description	journal (en) revista científica (es) ساینَسی رِسالہٕ (ks) مجلة (ar) revue scientifique (fr) rivista scientifica (it) науковий журнал (uk) wissenschaftliche Fachzeitschrift (de) wetenschappelijk tijdschrift van Lippincott Williams & Wilkins (nl)
language of work or name	wds:Q15762782-3DD6D696-9609-419E-92CC-FA0C40198664
language of work or name	English
OpenCitations bibliographic resource ID	wds:Q15762782-AEE5A2A1-435D-47A3-BD7C-61C1893C88CF
Crossref journal ID	wds:Q15762782-9548D077-CCAB-4B82-9BF6-ED38CA262E9D
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/439388
OpenCitations bibliographic resource ID	439388
Crossref journal ID	20900
rdfs:label	Clinical Dysmorphology (en) Clinical Dysmorphology (es) Clinical Dysmorphology (it) Clinical Dysmorphology (nl) Clinical Dysmorphology (ast)
skos:prefLabel	Clinical Dysmorphology (en) Clinical Dysmorphology (es) Clinical Dysmorphology (it) Clinical Dysmorphology (nl) Clinical Dysmorphology (ast)
name	Clinical Dysmorphology (en) Clinical Dysmorphology (es) Clinical Dysmorphology (it) Clinical Dysmorphology (nl) Clinical Dysmorphology (ast)
title	wds:Q15762782-519E9C02-9F7E-4D27-B355-3A652015CA85
title	Clinical Dysmorphology (en)
ERA Journal ID	wds:Q15762782-57D5D289-92CA-4FF8-91BA-7858A40C5D16
JUFO ID	wds:Q15762782-699D7FE4-3EC4-46BC-89FA-855A552A4CF1
ERA Journal ID	15918
JUFO ID	53575
NLM Unique ID	wds:Q15762782-89A21B2F-FF60-4587-B94D-32FEEA26758D
ACNP journal ID	wds:Q15762782-59BBCB5F-8F50-4CED-8309-6B0B6F0E846E wds:Q15762782-970BF3EE-AE97-40E8-88A5-FC6BF9BC12F4
HAL journal ID	wds:Q15762782-2F6BE709-9713-4833-B52D-E6F028040BC4
NLM Unique ID	9207893
ACNP journal ID	926274 2495601
HAL journal ID	11773
instance of	wds:Q15762782-31D622D9-2F23-488F-A2BD-17C712E84891
instance of	scientific journal
publisher	wds:Q15762782-6973EE84-C102-4644-9FA1-F68B3F6F70E8
publisher	Lippincott Williams & Wilkins
OpenAlex ID	wds:Q15762782-0AFC39E6-1372-45FB-9399-2D05056F71B1
country of origin	wds:Q15762782-A36EA4DF-5BA5-41CA-83D3-6AFA4F8BFDAA
official website	wds:Q15762782-17444F0D-F4B1-4B00-A135-BB7876DC48B8 wds:Q15762782-31ECC49E-1865-4741-96F2-DE908FC30E85 wds:Q15762782-BC9CECD2-A379-47A9-924D-A2CC974592BE
OpenAlex ID	V29023056
country of origin	United Kingdom
official website	http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00019605-000000000-00000 http://journals.lww.com/clindysmorphol/pages/default.aspx http://firstsearch.oclc.org/journal=0962-8827;screen=info;ECOIP
Scopus source ID	wds:Q15762782-103BE4D9-9229-4386-A547-9387217577CB
ISSN	wds:Q15762782-22B70CEF-45F4-43A6-A3F8-8241D63B774F wds:Q15762782-645B6C4E-EE21-44D1-9A87-BCC16F594A84
ISSN-L	wds:Q15762782-976794D4-1DCD-4AC0-A9C0-B19040D80B41
indexed in bibliographic review	wds:Q15762782-1031192E-DAF4-4763-A52B-B29F6259D82E wds:Q15762782-403DFB39-64FA-492B-A8E0-F27C1DED61D8
ISSN	urn:ISSN:0962-8827 urn:ISSN:1473-5717
ISSN-L	http://issn.org/resource/ISSN/0962-8827
Scopus source ID	21100240300
ISSN	0962-8827 1473-5717
ISSN-L	0962-8827
indexed in bibliographic review	Scopus Science Citation Index Expanded
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q15762782
is published in of	FGFR1 Pfeiffer syndrome without craniosynostosis: an additional case report The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation X-linked inheritance of Dandy-Walker variant Ophthalmic manifestations of Allgrove syndrome: report of a case Specific acromesomelia with facial and renal anomalies: a new syndrome The fetal mycophenolate mofetil syndrome The Jarcho-Levin syndrome (spondylocostal dysplasia) and complex congenital heart disease: a case report Two patients with varying combinations of sternal cleft, haemangiomas, midline abdominal raphe, coarctation of the aorta with a right aortic arch Molecular pathology of filamin A: diverse phenotypes, many functions. Cranio-osteoarthropathy in sibs Pitt-Hopkins syndrome in two patients and further definition of the phenotype A case of mosaic trisomy 19q12-q13.2 with high BMI, macrocephaly, and speech delay: does USF2 determine size in the 19q phenotypes? A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Warburg Micro syndrome in a Turkish boy. Cri-du-chat syndrome associated with arachnoid cyst causing triventricular hydrocephalus. Double dens invaginatus of molarized maxillary central incisors, premolarization of maxillary lateral incisors, multituberculism of the mandibular incisors, canines and first premolar, and sensorineural hearing loss Floating-Harbor Syndrome New syndrome: clavicle hypoplasia, facial dysmorphism, severe myopia, single central incisor and peripheral neuropathy Solitary median maxillary central incisor, Duane retraction syndrome, growth hormone deficiency and duplicated thumb phalanx: a case report Hirschsprung disease, mental retardation and dysmorphic facial features in five unrelated children Goldberg-Shprintzen syndrome: report of a new family and review of the literature Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome). Distichiasis-lymphoedema syndrome: a family report Townes-Brocks syndrome presenting as end stage renal failure

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