Literature DB >> 15444577

[Hereditary abnormality of the buccal mucosa: abnormal bands and frenula].

J PSAUME.   

Abstract

Keywords:  ABNORMALITIES; MOUTH

Mesh：

Year:  1954        PMID： 15444577

Source DB:  PubMed          Journal:  Revue Stomatol


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  23 in total

1.  Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter.

Authors:  K PATAU; E THERMAN; S L INHORN; D W SMITH; A L RUESS
Journal:  Chromosoma       Date:  1961       Impact factor: 4.316

2.  [Syndrome patients within the framework of the early orthodontic treatment of infants with cheilognathopalatoschisis].

Authors:  M Bacher; P Koppenburg; E Leidig; D Dausch-Neumann; N Schwenzer; H G Döring
Journal:  Fortschr Kieferorthop       Date:  1989-12

3.  Mohr-Claussen Syndrome: A Rare Case.

Authors:  Manjiri Uttam Joshi; Namish Jagdish Chandra Batra; Ankita Pradeep Patel
Journal:  J Clin Diagn Res       Date:  2016-10-01

4.  Rare case of orofaciodigital syndrome type I.

Authors:  Abhishek Bahadur Singh; Manish Girhotra; Medha Goel; Shilpee Bhatia
Journal:  BMJ Case Rep       Date:  2013-02-14

5.  The orofaciodigital (OFD) syndromes.

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

6.  [The differential diagnosis of Papillon-Lénge-Psaume-syndrome and Mohr's syndrome].

Authors:  W Fuhrmann; A Stahl
Journal:  Humangenetik       Date:  1970

7.  Fibrocystic disease of liver and pancreas; under-recognized features of the X-linked ciliopathy oral-facial-digital syndrome type 1 (OFD I).

Authors:  Shilpa Chetty-John; Katie Piwnica-Worms; Joy Bryant; Isa Bernardini; Roxanne E Fischer; Theo Heller; William A Gahl; Meral Gunay-Aygun
Journal:  Am J Med Genet A       Date:  2010-10       Impact factor: 2.802

8.  Orofaciodigital syndrome type III in two sibs.

Authors:  R A Smith; D Gardner-Medwin
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

9.  Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variability.

Authors:  Izak J Bisschoff; Christine Zeschnigk; Denise Horn; Brigitte Wellek; Angelika Rieß; Maja Wessels; Patrick Willems; Peter Jensen; Andreas Busche; Jens Bekkebraten; Maya Chopra; Hanne Dahlgaard Hove; Christina Evers; Ketil Heimdal; Ann-Sophie Kaiser; Erdmut Kunstmann; Kristina Lagerstedt Robinson; Maja Linné; Patricia Martin; James McGrath; Winnie Pradel; Katrina E Prescott; Bernd Roesler; Gorazd Rudolf; Ulrike Siebers-Renelt; Nataliya Tyshchenko; Dagmar Wieczorek; Gerhard Wolff; William B Dobyns; Deborah J Morris-Rosendahl
Journal:  Hum Mutat       Date:  2012-10-17       Impact factor: 4.878

10.  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
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