About: International nosology of heritable disorders of connective tissue, Berlin, 1986

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1988 (uk) im März 1988 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57752688-1DEBF06F-42BC-43C9-B5AF-F4D630960B4F
publication date	1988-03-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q57752688-07D5DEF3-5FBD-48B2-9D86-0523DEBD76C0 wds:Q57752688-4C7FC18C-1176-411C-A890-C235485AF369 wds:Q57752688-59B1D989-5D63-4EF0-B74B-A905C9DAD541 wds:Q57752688-5B1AAABE-2048-42E8-840D-4CA745D94DF4 wds:Q57752688-634CBCD4-D59F-4E2C-AA54-8395E68E8D6E wds:Q57752688-6554E987-D894-424E-8066-1A6AA8469D34 wds:Q57752688-67D40C2C-BA37-4550-9413-CA4FE60ACE2A wds:Q57752688-6CFBCC64-09C7-4008-A0F6-B4989CA1A181 wds:Q57752688-76DB5FEB-4ACC-4815-B10C-281B8DB72E2D wds:Q57752688-782A6583-F500-41F1-9DF6-3A461757064F wds:Q57752688-8DF4090C-BE70-42E5-9967-0CE9CB1D9DFE wds:Q57752688-9AD73B4C-9DA3-4F79-890D-1BF5EA772042 wds:Q57752688-AB392BCB-4B50-44E4-B0ED-1796D6695F32 wds:Q57752688-B22D4181-D6FF-4744-B70C-606AA0EFF18E wds:Q57752688-B66BD5FA-C290-4164-858D-BA992F283C7A wds:Q57752688-B85A1A0D-C0B1-4739-A6BB-8290A483512E wds:Q57752688-C2D0943C-41EA-48D8-9FAD-9E4BC9C5B093 wds:Q57752688-D38D43BE-35C9-4987-B919-6CECD4B1BED5 wds:Q57752688-E6B55BB7-1A68-4976-8417-58EAEA5DCF28 wds:Q57752688-E7E7F8F7-2773-4D76-A89A-B5951A7AE33B
author name string	V. A. McKusick R. Goodman P. Beighton F. M. Pope D. W. Hollister J. G. Hall G. Finidori T. Gedde-Dahl I. Young E. Thompson J. W. Spranger D. Sillence James F. Reynolds W. Horton D. Danks R. E. Pyeritz I. Winship P. Tsipouras D. Viljoen A. de Paepe
rdfs:label	International nosology of heritable disorders of connective tissue, Berlin, 1986 (en) International nosology of heritable disorders of connective tissue, Berlin, 1986 (nl)
skos:prefLabel	International nosology of heritable disorders of connective tissue, Berlin, 1986 (en) International nosology of heritable disorders of connective tissue, Berlin, 1986 (nl)
name	International nosology of heritable disorders of connective tissue, Berlin, 1986 (en) International nosology of heritable disorders of connective tissue, Berlin, 1986 (nl)
author	wds:Q57752688-2B4B9F8B-BD1E-4655-B033-CE5EFAAE25E7 wds:Q57752688-2C7937EB-9235-475C-8B7F-314F803B603B
author	David Rimoin John Marius Opitz
title	wds:Q57752688-85E40583-3C9E-4E95-AE70-703D56FF61F9
title	International nosology of heritable disorders of connective tissue, Berlin, 1986 (en)
page(s)	wds:Q57752688-74BE4C38-8D00-44FB-AD4C-718CB8267600
page(s)	581-594
instance of	wds:Q57752688-0699C75A-F111-4034-B720-4D391F39D5C6
instance of	scholarly article
main subject	wds:Q57752688-5FACFF3B-6370-42C2-8675-133871DEA515
main subject	connective tissue
PubMed ID	wds:Q57752688-9D3B4F04-F7CF-43BD-B8D2-8CD491812EC9
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3287925
PubMed ID	3287925
published in	wds:Q57752688-6302F3D2-FA99-4FD4-885D-0C9F50AC3DE8
published in	American Journal of Medical Genetics Part A
issue	wds:Q57752688-400FFCFE-3D03-4FC2-9616-E4409DB8304F
volume	wds:Q57752688-72619E00-EC09-450D-A299-8C94FCAA94B5
issue	3
volume	29
DOI	wds:Q57752688-86D6A062-5A77-435D-9654-3F906432DC81
DOI	http://dx.doi.org/10.1002/AJMG.1320290316
DOI	10.1002/AJMG.1320290316
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57752688
is cites work of	Marfan syndrome: current perspectives Neurovascular manifestations of connective-tissue diseases: A review Genetics of thoracic aortic aneurysm: at the crossroad of transforming growth factor-β signaling and vascular smooth muscle cell contractility Spontaneous rupture of the femoral arteries Multiple molecular mechanisms underlying subdiagnostic variants of Marfan syndrome The clinical spectrum of complete FBN1 allele deletions Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type Musculoskeletal complaints, physical activity and health-related quality of life among patients with the Ehlers-Danlos syndrome hypermobility type. The new Ghent criteria for Marfan syndrome: what do they change? The molecular genetics of the Ehlers-Danlos syndrome Ehlers-Danlos syndrome has varied molecular mechanisms Missing inferior labial and lingual frenula in Ehlers-Danlos syndrome Ehlers-Danlos syndrome with a spontaneous caroticocavernous fistula occluded by detachable balloon: case report and review of literature Detection of abnormal aortic elastic properties in asymptomatic patients with Marfan syndrome by combined transoesophageal echocardiography and acoustic quantification Marfan syndrome: what internists and pediatric or adult cardiologists need to know Aortic distensibility and stiffness index measured by magnetic resonance imaging in patients with Marfan's syndrome Abnormal mechanical properties of the aorta in Marfan's syndrome. Heterogeneous aortic response to acute β-adrenergic blockade in Marfan syndrome The Marfan syndrome: abnormal aortic elastic properties Marfan's syndrome Fibrillln mutations in Marfan syndrome and related phenotypes A point mutation in an intronic branch site results in aberrant splicing of COL5A1 and in Ehlers-Danlos syndrome type II in two British families Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families

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