Literature DB >> 7127881

Hyperphalangy and clinodactyly of the index finger with Pierre Robin anomaly: Catel-Manzke syndrome. A case report and review of the literature.

V Sundaram, K Taysi, A F Hartmann, G D Shackelford, J P Keating.   

Abstract

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Year:  1982        PMID： 7127881     DOI： 10.1111/j.1399-0004.1982.tb01395.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

1.  A male infant with the Catel-Manzke syndrome and dislocatable knees.

Authors:  E M Thompson; R M Winter; M J Williams
Journal:  J Med Genet       Date:  1986-06       Impact factor: 6.318

2.  Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.

Authors:  Nadja Ehmke; Almuth Caliebe; Rainer Koenig; Sarina G Kant; Zornitza Stark; Valérie Cormier-Daire; Dagmar Wieczorek; Gabriele Gillessen-Kaesbach; Kirstin Hoff; Amit Kawalia; Holger Thiele; Janine Altmüller; Björn Fischer-Zirnsak; Alexej Knaus; Na Zhu; Verena Heinrich; Celine Huber; Izabela Harabula; Malte Spielmann; Denise Horn; Uwe Kornak; Jochen Hecht; Peter M Krawitz; Peter Nürnberg; Reiner Siebert; Hermann Manzke; Stefan Mundlos
Journal:  Am J Hum Genet       Date:  2014-12-04       Impact factor: 11.025

3.  Pierre Robin sequence and hyperphalangy--a genetic entity (Catel-Manzke syndrome).

Authors:  E Brude
Journal:  Eur J Pediatr       Date:  1984-08       Impact factor: 3.183

4.  Catel-Manzke Syndrome: Further Delineation of the Phenotype Associated with Pathogenic Variants in TGDS.

Authors:  Rachel Pferdehirt; Mahim Jain; Maria A Blazo; Brendan Lee; Lindsay C Burrage
Journal:  Mol Genet Metab Rep       Date:  2015-09-01
  4 in total

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