Literature DB >> 1201338

The Coffin-Lowry syndrome: a simply inherited trait comprising mental retardation, faciodigital anomalies and skeletal involvement.

S A Temtamy, J D Miller, J P Dorst, I Hussels-Maumenee, C Salinas, Y Lacassie, K R Kenyon.   

Abstract

Entities:  

Mesh：

Year:  1975        PMID： 1201338

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


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  4 in total

1.  Coffin-Lowry syndrome.

Authors:  Sanjeev R Ahuja; Shubhangi Upadhye; Hemant V Kulkarni; Madhuri V Kulkarni
Journal:  Indian J Pediatr       Date:  2003-12       Impact factor: 1.967

2.  The Coffin-Lowry syndrome. A study of two new index patients and their families.

Authors:  M Haspeslagh; J P Fryns; L Beusen; F Van Dessel; L Vinken; E Moens; H Van den Berghe
Journal:  Eur J Pediatr       Date:  1984-12       Impact factor: 3.183

3.  Phenotypic and evolutionary implications of modulating the ERK-MAPK cascade using the dentition as a model.

Authors:  Pauline Marangoni; Cyril Charles; Paul Tafforeau; Virginie Laugel-Haushalter; Adriane Joo; Agnès Bloch-Zupan; Ophir D Klein; Laurent Viriot
Journal:  Sci Rep       Date:  2015-06-30       Impact factor: 4.379

4.  RSK2 is a modulator of craniofacial development.

Authors:  Virginie Laugel-Haushalter; Marie Paschaki; Pauline Marangoni; Coralie Pilgram; Arnaud Langer; Thibaut Kuntz; Julie Demassue; Supawich Morkmued; Philippe Choquet; André Constantinesco; Fabien Bornert; Matthieu Schmittbuhl; Solange Pannetier; Laurent Viriot; André Hanauer; Pascal Dollé; Agnès Bloch-Zupan
Journal:  PLoS One       Date:  2014-01-08       Impact factor: 3.240
  4 in total

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