A 6-year-old child with Fryns syndrome: Further delineation of the natural history of the condition in survivors
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference24 articles.
1. Fryns syndrome: report on 8 new cases;Aymé;Clin. Genet.,1989
2. Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome;Bamforth;Am. J. Med. Genet.,1989
3. Fryns syndrome: two further cases without lateral diaphragmatic defects;Bartsch;Clin. Dysmorphol.,1995
4. Apparent Fryns syndrome in a boy with a tandem duplication of 1q24-31.2;Clark;Am. J. Med. Genet.,1989
5. Ocular findings in Fryns syndrome;Coursiefen;Acta Ophthalmol. Scand.,2000
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Challenging Anaesthesia Management of a Patient with Fryns Syndrome: A Case Report;Turkish Journal of Anaesthesiology and Reanimation;2023-06-01
2. Extracorporeal Membrane Oxygenation in Premature Infants With Congenital Diaphragmatic Hernia;ASAIO Journal;2018-09
3. Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndrome;European Journal of Human Genetics;2018-01-12
4. Fryns Syndrome;Obstetric Imaging: Fetal Diagnosis and Care;2018
5. Fryns Syndrome;Diagnostic Imaging: Obstetrics;2016
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