Chromosome 1p31.1p31.3 Deletion in a Patient with Craniosynostosis, Central Nervous System and Renal Malformation: Case Report and Review of the Literature-Reference-Cited by-同舟云学术

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Chromosome 1p31.1p31.3 Deletion in a Patient with Craniosynostosis, Central Nervous System and Renal Malformation: Case Report and Review of the Literature

Published:2016-11-17 Issue:1 Volume:8 Page:30-35
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Rivera-Pedroza Carlos I.,Barraza-García Jimena,Paumard-Hernández Beatriz,Nevado Julian,Orbea-Gallardo Carlos,Sánchez del Pozo Jaime,Heath Karen E.

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics

Cited by 8 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. Novel genetic syndrome manifesting with cerebral atrophy, cataract, hypoacusis, diabetes, and brachy-/syndactyly;Journal of Family Medicine and Primary Care;2023-12

2. Conserved Molecular Players Involved in Human Nose Morphogenesis Underlie Evolution of the Exaggerated Snout Phenotype in Cichlids;Genome Biology and Evolution;2023-03-17

3. Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles;Italian Journal of Pediatrics;2022-03-04

4. Parallel molecular mechanisms underlie convergent evolution of the exaggerated snout phenotype in East African cichlids;2022-01-14

5. Chromosome 1p31.1 Deletion Syndrome: Limited Expression;Annals of Indian Academy of Neurology;2021

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