Literature DB >> 526577

Clinical variability in the Marfan syndrome(s).

R E Pyeritz, E A Murphy, V A McKusick.   

Abstract

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Mesh：

Year:  1979        PMID： 526577

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  8 in total

1.  Linkage data for Marfan syndrome and markers on chromosomes 1 and 11.

Authors:  J de Groote; P A Farndon; M V Kilpatrick; A de Paepe; J W Oorthuys; N C Nevin; A H Child; F M Pope
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

2.  Diagnosing Marfan syndrome.

Authors:  M Super
Journal:  Br Med J (Clin Res Ed)       Date:  1988-05-14

3.  Ascertainment and severity of Marfan syndrome in a Scottish population.

Authors:  J R Gray; A B Bridges; M J Faed; T Pringle; P Baines; J Dean; M Boxer
Journal:  J Med Genet       Date:  1994-01       Impact factor: 6.318

4.  The Marfan syndrome--analysis of growth and cardiovascular manifestation.

Authors:  U Vetter; R Mayerhofer; D Lang; G von Bernuth; M B Ranke; A A Schmaltz
Journal:  Eur J Pediatr       Date:  1990-04       Impact factor: 3.183

5.  A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression.

Authors:  Bruno L Lima; Enrico J C Santos; Gustavo R Fernandes; Christian Merkel; Marco R B Mello; Juliana P A Gomes; Marina Soukoyan; Alexandre Kerkis; Silvia M G Massironi; José A Visintin; Lygia V Pereira
Journal:  PLoS One       Date:  2010-11-30       Impact factor: 3.240

6.  Marfan's syndrome. Broad spectral surgical treatment cardiovascular manifestations.

Authors:  E S Crawford
Journal:  Ann Surg       Date:  1983-10       Impact factor: 12.969

7.  Homozygosity for autosomal dominant Marfan syndrome.

Authors:  J Chemke; R Nisani; A Feigl; R Garty; M Cooper; Y Bårash; D Duksin
Journal:  J Med Genet       Date:  1984-06       Impact factor: 6.318

8.  An infant with Marfanoid phenotype and congenital contractures associated with ocular and cardiovascular anomalies, cerebral white matter hypoplasia and spinal axonopathy.

Authors:  P Tamminga; F G Jennekens; P G Barth; P Fleury; H van den Berg; J W Oorthuys
Journal:  Eur J Pediatr       Date:  1985-01       Impact factor: 3.183
  8 in total

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