Literature DB >> 5146584

Syndrome characterized by lingual malformation, polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome).

K H Gustavson, A Kreuger, P O Petersson.   

Abstract

Entities:  

Mesh：

Year:  1971        PMID： 5146584     DOI： 10.1111/j.1399-0004.1971.tb00287.x

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


× No keyword cloud information.
  10 in total

1.  Central nervous system malformations in Mohr's syndrome.

Authors:  W Reardon; M G Harbord; M A Hall-Craggs; B Kendall; E M Brett; M Baraitser
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

2.  Genetic aspects of congenital cerebellar ataxia.

Authors:  D Kumar
Journal:  Indian J Pediatr       Date:  1986 Nov-Dec       Impact factor: 1.967

3.  The orofaciodigital (OFD) syndromes.

Authors:  M Baraitser
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318

4.  Joubert-Boltshauser syndrome with polydactyly in siblings.

Authors:  J Egger; M H Bellman; E M Ross; M Baraitser
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-08       Impact factor: 10.154

5.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

6.  Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.

Authors:  V Váradi; L Szabó; Z Papp
Journal:  J Med Genet       Date:  1980-04       Impact factor: 6.318

7.  Joubert's syndrome with retinal dysplasia: neonatal tachypnoea as the clue to a genetic brain-eye malformation.

Authors:  M D King; J Dudgeon; J B Stephenson
Journal:  Arch Dis Child       Date:  1984-08       Impact factor: 3.791

8.  Orocardiodigital syndrome: an oral-facial-digital type II variant associated with atrioventricular canal.

Authors:  M C Digilio; B Marino; A Giannotti; B Dallapiccola
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

9.  Oral-facial-digital syndrome type 1 in males: Congenital heart defects are included in its phenotypic spectrum.

Authors:  Arjan Bouman; Mariëlle Alders; Roelof Jan Oostra; Elisabeth van Leeuwen; Nikki Thuijs; Anne-Marie van der Kevie-Kersemaekers; Merel van Maarle
Journal:  Am J Med Genet A       Date:  2017-04-03       Impact factor: 2.802

Review 10.  Genetics of atrioventricular canal defects.

Authors:  Flaminia Pugnaloni; Maria Cristina Digilio; Carolina Putotto; Enrica De Luca; Bruno Marino; Paolo Versacci
Journal:  Ital J Pediatr       Date:  2020-05-13       Impact factor: 2.638
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.