Literature DB >> 27439648

FOXF1 gene mutation in alveolar capillary dysplasia associated with Hirschsprung's disease and clinical review.

Dimple Goel1,2, Ju Lee Oei1,2, Antonia W Shand2,3, David Mowat2,4, Christine Loo5,6.   

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Year:  2016        PMID： 27439648     DOI： 10.1111/jpc.13191

Source DB:  PubMed          Journal:  J Paediatr Child Health        ISSN： 1034-4810            Impact factor:   1.954


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  4 in total

1.  Two autopsy cases of siblings with alveolar capillary dysplasia: clinical and post-mortem issues.

Authors:  Caterina Petetta; Lucia Tattoli; Giovanni Botta; Giancarlo Di Vella
Journal:  Forensic Sci Med Pathol       Date:  2019-09-11       Impact factor: 2.007

Review 2.  Recognizing genetic disease: A key aspect of pediatric pulmonary care.

Authors:  Lael M Yonker; Megan H Hawley; Peter P Moschovis; Mengdi Lu; T Bernard Kinane
Journal:  Pediatr Pulmonol       Date:  2020-07

3.  Antenatal gastrointestinal anomalies in neonates subsequently found to have alveolar capillary dysplasia.

Authors:  Dimple Goel; Ju Lee Oei; Kei Lui; Meredith Ward; Antonia W Shand; David Mowat; Andrew J Gifford; Christine Loo
Journal:  Clin Case Rep       Date:  2017-03-13

4.  The regulatory roles and mechanisms of the transcription factor FOXF2 in human diseases.

Authors:  Qiong Wu; Wei Li; Chongge You
Journal:  PeerJ       Date:  2021-03-02       Impact factor: 2.984
  4 in total

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