Literature DB >> 20512033

Consideration of VACTERL association in patients with trisomy 21.

Benjamin D Solomon1, Sophia M Bous, Simona Bianconi, Daniel E Pineda-Alvarez.   

Abstract

Entities:  

Mesh：

Year:  2010        PMID： 20512033      PMCID： PMC2933298          DOI： 10.1097/MCD.0b013e32833b2b9c

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  6 in total

1.  Evidence for inheritance in patients with VACTERL association.

Authors:  Benjamin D Solomon; Daniel E Pineda-Alvarez; Manu S Raam; Derek A T Cummings
Journal:  Hum Genet       Date:  2010-04-06       Impact factor: 4.132

2.  The spectrum of congenital anomalies of the VATER association: an international study.

Authors:  L D Botto; M J Khoury; P Mastroiacovo; E E Castilla; C A Moore; R Skjaerven; O M Mutchinick; B Borman; G Cocchi; A E Czeizel; J Goujard; L M Irgens; P A Lancaster; M L Martínez-Frías; P Merlob; A Ruusinen; C Stoll; Y Sumiyoshi
Journal:  Am J Med Genet       Date:  1997-07-11

3.  VATERL: an epidemiologic analysis of risk factors.

Authors:  M Rittler; J E Paz; E E Castilla
Journal:  Am J Med Genet       Date:  1997-12-12

4.  Down syndrome and scoliosis: a review of a 50-year experience at one institution.

Authors:  Todd A Milbrandt; Charles E Johnston
Journal:  Spine (Phila Pa 1976)       Date:  2005-09-15       Impact factor: 3.468

5.  Pattern of malformations in the axial skeleton in human trisomy 21 fetuses.

Authors:  J W Keeling; B F Hansen; I Kjaer
Journal:  Am J Med Genet       Date:  1997-02-11

6.  Congenital defects among liveborn infants with Down syndrome.

Authors:  Mario A Cleves; Charlotte A Hobbs; Phillip A Cleves; John M Tilford; T M Bird; James M Robbins
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2007-09
  6 in total
  4 in total

1.  VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations.

Authors:  E Brosens; H Eussen; Y van Bever; R M van der Helm; H Ijsselstijn; H P Zaveri; R Wijnen; D A Scott; D Tibboel; A de Klein
Journal:  Mol Syndromol       Date:  2013-02

2.  Mitochondrial Factors and VACTERL Association-Related Congenital Malformations.

Authors:  S Siebel; B D Solomon
Journal:  Mol Syndromol       Date:  2013-02

3.  Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association.

Authors:  Nneamaka B Agochukwu; Daniel E Pineda-Alvarez; Amelia A Keaton; Nicole Warren-Mora; Manu S Raam; Aparna Kamat; Settara C Chandrasekharappa; Benjamin D Solomon
Journal:  Eur J Med Genet       Date:  2011-02-26       Impact factor: 2.708

4.  A Network of Anomalies Prompting VACTERL Workup in a Trisomy 21 Newborn.

Authors:  Trenton Reinicke; Christina L Costantino; Danyon J Anderson; Jacqueline Tran; Cornelia Griggs
Journal:  Cureus       Date:  2022-01-16
  4 in total

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