Literature DB >> 5047651

[The Pierre Robin syndrome: unusual associated developmental defects].

W Holthusen.   

Abstract

Entities:  

Mesh：

Year:  1972        PMID： 5047651

Source DB:  PubMed          Journal:  Ann Radiol (Paris)        ISSN： 0003-4185


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  6 in total

1.  Pierre Robin syndrome: autosomal dominant inheritance with pleiotropic effect.

Authors:  S S Sidhu; R N Deshmukh
Journal:  Indian J Pediatr       Date:  1989 May-Jun       Impact factor: 1.967

2.  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

3.  A digitopalatal syndrome with associated anomalies of the heart, face, and skeleton.

Authors:  R E Stevenson; H A Taylor; O M Burton; H B Hearn
Journal:  J Med Genet       Date:  1980-06       Impact factor: 6.318

4.  Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndrome.

Authors:  M C Silengo; P Franceschini; A Cerutti; C Fabris
Journal:  Pediatr Radiol       Date:  1977-10-28

5.  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

6.  Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence.

Authors:  M Gewitz; R Dinwiddie; T Yuille; F Hill; C O Carter
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318
  6 in total

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