Child with velocardiofacial syndrome and del (4)(q34.2): Another critical region associated with a velocardiofacial syndrome-like phenotype
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference24 articles.
1. Case Report: Two newborns with chromosome 4 imbalances: deletion 4q33 → q35 and ring r (4) (pterq35.2-qter)
2. Mild phenotypic manifestations of terminal deletion of the long arm of chromosome 4: clinical description of a new patient
3. Interstitial deletion, del(4)(q33q35.1), in a mother and two children.
4. Terminal deletion of the long arm of chromosome 4 in a mother and two sons
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3. Analysis of genetic characteristics of 436 children with dysplasia and detailed analysis of rare karyotype;Open Life Sciences;2022-01-01
4. Cytogenomic characterization of a de novo 4q34.1 deletion in a girl with mild dysmorphic features and a coagulation disorder;Molecular Cytogenetics;2021-09-04
5. SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients;eLife;2021-06-08
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