Literature DB >> 5002154

Glossoptotic hypoxia and micrognathia--the Pierre Robin syndrome reviewed. Early recognition and prompt surgical treatment is important for survival.

P B Farnsworth, P T Pacik.   

Abstract

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Year:  1971        PMID： 5002154     DOI： 10.1177/000992287101001029

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN： 0009-9228            Impact factor:   1.168


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  5 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.  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

3.  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

4.  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

5.  Proximal femoral focal deficiency associated with the Robin anomalad.

Authors:  E R Graviss; P A Monteleone; L R Wampler; M J Silberstein; A E Brodeur
Journal:  J Med Genet       Date:  1980-10       Impact factor: 6.318
  5 in total

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