Phenotypic correlations in patients with ring chromosome 22-Reference-Cited by-同舟云学术

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Phenotypic correlations in patients with ring chromosome 22

Published:2008-04-23 Issue:4 Volume:12 Page:239-249
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Hunter A. G. W.,Ray M.,Wang H. S.,Thompson D. R.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1977.tb00933.x/fullpdf

Reference26 articles.

1. Trisomy 21 or 22 in Down's syndrome;Back;Lancet,1967

2. A patient with 45, XX, G-/46, XX, Gr mosaicism;Bank;J. med. Genet.,1969

3. A case of ring chromosome (322);Brookfield;J. med Genet.,1976

4. G-deletion syndrome II;Chauvel;Hum. Genet.,1972

5. Identification of 21r and 22r chromosomes by quinacrine fluorescence;Crandall;Clin. Genet.,1972

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1. Ring Chromosome 22;Human Ring Chromosomes;2024

2. Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes;Nature Reviews Neurology;2023-11-24

3. Neurofibromatosis type 2 in Phelan-McDermid syndrome: Institutional experience and review of the literature;European Journal of Medical Genetics;2020-11

4. Phelan–McDermid Syndrome;Neuronal and Synaptic Dysfunction in Autism Spectrum Disorder and Intellectual Disability;2016

5. Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion;American Journal of Medical Genetics Part A;2014-04-03

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