Literature DB >> 160752

Terminological, diagnostic, nosological, and anatomical-developmental aspects of developmental defects in man.

J M Opitz, J Herrmann, J C Pettersen, E T Bersu, S C Colacino.   

Abstract

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Mesh：

Year:  1979        PMID： 160752     DOI： 10.1007/978-1-4615-8276-2_2

Source DB:  PubMed          Journal:  Adv Hum Genet        ISSN： 0065-275X


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  13 in total

Review 1.  Thalidomide embryopathy: a model for the study of congenital incomitant horizontal strabismus.

Authors:  M T Miller
Journal:  Trans Am Ophthalmol Soc       Date:  1991

2.  Overlap syndrome: a diagnostic dilemma.

Authors:  Kaushal Mahendra Shah; Sampada Kanitkar
Journal:  BMJ Case Rep       Date:  2012-11-27

Review 3.  Molecular approaches to dysmorphology.

Authors:  A Ivens; G Moore; R Williamson
Journal:  J Med Genet       Date:  1988-07       Impact factor: 6.318

4.  A new variant of the acrorenal syndrome associated with bilateral oligomeganephronic hypoplasia.

Authors:  M Miltényi; L Balogh; K Schmidt; Z Detre; T Hernády; A Czeizel
Journal:  Eur J Pediatr       Date:  1984-04       Impact factor: 3.183

5.  An aetiological study of the VACTERL-association.

Authors:  A Czeizel; I Ludányi
Journal:  Eur J Pediatr       Date:  1985-11       Impact factor: 3.183

6.  Frontonasal dysplasia as an expression of holoprosencephaly.

Authors:  M Roubicek; J Spranger; S Wende
Journal:  Eur J Pediatr       Date:  1981-10       Impact factor: 3.183

Review 7.  Congenital malformations: an inquiry into classification and nomenclature.

Authors:  H Kalter
Journal:  J Med Genet       Date:  1998-08       Impact factor: 6.318

8.  Spectrum of anomalies in Fanconi anaemia.

Authors:  A Glanz; F C Fraser
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

9.  Epidemiology of fractures in people with severe and profound developmental disabilities.

Authors:  Norris R Glick; Milton H Fischer; Dennis M Heisey; Glen E Leverson; David C Mann
Journal:  Osteoporos Int       Date:  2004-08-07       Impact factor: 4.507

10.  Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Authors:  R Faridi; A U Rehman; R J Morell; P L Friedman; L Demain; S Zahra; A A Khan; D Tohlob; M Z Assir; G Beaman; S N Khan; W G Newman; S Riazuddin; T B Friedman
Journal:  Clin Genet       Date:  2016-11-16       Impact factor: 4.438
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