Literature DB >> 1583665

Atypical case of Aarskog syndrome.

R V Mikelsaar1, I W Lurie.   

Abstract

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Year:  1992        PMID： 1583665      PMCID： PMC1015959          DOI： 10.1136/jmg.29.5.349

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  3 in total

1.  A familial syndrome of short stature associated with facial dysplasia and genital anomalies.

Authors:  D Aarskog
Journal:  J Pediatr       Date:  1970-11       Impact factor: 4.406

Review 2.  Autosomal dominant inheritance of the Aarskog syndrome.

Authors:  R E Grier; F H Farrington; R Kendig; P Mamunes
Journal:  Am J Med Genet       Date:  1983-05

3.  Anomalous cerebral venous drainage in Aarskog syndrome.

Authors:  P van den Bergh; J P Fryns; G Wilms; R Piot; G Dralands; R van den Bergh
Journal:  Clin Genet       Date:  1984-03       Impact factor: 4.438
  3 in total
  3 in total

1.  Identifying Aarskog Syndrome.

Authors:  Anis Ahmed; Abdullah Mufeed; Ashir Kolikkal Ramachamparambathu; Umer Hasoon
Journal:  J Clin Diagn Res       Date:  2016-12-01

2.  Cerebrovascular disease associated with Aarskog-Scott syndrome.

Authors:  Michael L Diluna; Nduka M Amankulor; Michele H Johnson; Murat Gunel
Journal:  Neuroradiology       Date:  2007-02-10       Impact factor: 2.995

3.  Identification of novel mutations in Mexican patients with Aarskog-Scott syndrome.

Authors:  Mariana Pérez-Coria; José J Lugo-Trampe; Michell Zamudio-Osuna; Iram P Rodríguez-Sánchez; Angel Lugo-Trampe; Beatriz de la Fuente-Cortez; Luis D Campos-Acevedo; Laura E Martínez-de-Villarreal
Journal:  Mol Genet Genomic Med       Date:  2015-02-17       Impact factor: 2.183
  3 in total

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