Ring Chromosome 22
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-47530-6_26
Reference120 articles.
1. Ahn H, Seo GH. Keum C, Heo SH, Kim T, Choi J, Yum MS, Lee BH (2020) Diagnosis of metachromatic leukodystrophy in a patient with regression and Phelan-McDermid syndrome. Brain Dev 42(5):414–417.https://doi.org/10.1016/j.braindev.2020.02.003
2. Aller V, Abrisqueta JA, de Torres ML, Martin-Lucas MA, Perez-Castillo A, Del Mazo J (1979) An r(22)(p11→q13) in a moderately mentally retarded girl. Hum Genet 51(2):157–162. https://doi.org/10.1007/BF00287170
3. Arinami T, Kondo I, Hamaguchi H, Nakajima S (1986) Multifocal meningiomas in a patient with a constitutional ring chromosome 22. J Med Genet 23(2):178–180. https://doi.org/10.1136/jmg.23.2.178
4. Assumpcao FB Jr (1998) Brief report: A case of chromosome 22 alteration associated with autistic syndrome. J Autism Dev Disord 28(3):253–256. https://doi.org/10.1023/a:1026025606967
5. Battini R, Battaglia A, Bertini V, Cioni G, Parrini B, Rapalini E, Simi P, Tinelli F, Valetto A (2004) Characterization of the phenotype and definition of the deletion in a new patient with ring chromosome 22. Am J Med Genet 130A(2):196–199. https://doi.org/10.1002/ajmg.a.30276
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