Case Report Familial balanced translocation leading to an offspring with phenotypic manifestations of 9p syndrome-Reference-Cited by-同舟云学术

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Case Report Familial balanced translocation leading to an offspring with phenotypic manifestations of 9p syndrome

Published:2014 Issue:2 Volume:13 Page:4302-4310
ISSN:1676-5680
Container-title:Genetics and Molecular Research
language:
Short-container-title:Genet. Mol. Res.

Author:

Abreu L.S.,Brassesco M.S.,Moreira M.L.C.,Pina-Neto J.M.

Publisher

Genetics and Molecular Research

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.funpecrp.com.br/gmr/year2014/vol13-2/pdf/gmr3782.pdf

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. Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly;Molecular Genetics & Genomic Medicine;2021-10-05

2. Anaesthesia recommendations for Deletion 9p syndrome;ANASTH INTENSIVMED;2021

3. Identification of a possible association of JAK2 in development of microphthalmia, anophthalmia, and coloboma (MAC) complex in a child with 9p deletion and duplication;Ophthalmic Genetics;2020-06-08

4. Subtelomeric Rearrangements in Patients with Recurrent Miscarriage;INT J FERTIL STERIL;2018

5. Neonatal hyperinsulinemic hypoglycemia in a patient with 9p deletion syndrome;European Journal of Medical Genetics;2018-08

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