Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature
Author:
Affiliation:
1. Human Cytogenetics Department National Research Centre Cairo Egypt
2. Clinical Genetics Department National Research Centre Cairo Egypt
3. Pediatric Department Faculty of Medicine Fayoum unIversity Fayoum Egypt
Publisher
Wiley
Subject
Genetics (clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1546
Reference73 articles.
1. Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf–Hirschhorn Syndrome
2. Growth charts for Wolf-Hirschhorn syndrome (0–4 years of age)
3. Uncommon Oral Cleft in Wolf-Hirschhorn Syndrome
4. Ring chromosome 4 and Wolf‐Hirschhorn syndrome (WHS) in a child with multiple anomalies;Balci S.;American Journal of Medical Genetics. Part A,2006
5. Natural history of Wolf‐Hirschhorn Syndrome: Experience with 15 cases;Battaglia A.;Pediatrics,1999
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