Two rare cases of 6p partial deletion
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb03188.x/fullpdf
Reference6 articles.
1. Rearrangements of the short arm of chromosome No. 6 in T-cell lymphomas;Mecucci;Leukemia Res.,1985
2. The short arm of chromosome 6 is nonrandomly rearranged in secondary myelodysplastic syndromes;Mecucci;Cancer Genet. Cytogenet.,1988
3. Gene dosage effects for coagulation factors XII (F12) and XIII subunit A (F13A) in a case with partial monosomy 6p resulting from a maternal pericentric inversion of chromosome 6;Navahara;Jpn. J. Hum. Genet.,1987
4. Clinical evidence for localization of HLA proximal of chromosome 6p22;Sachs;Lancet,1983
5. A patient with an interstitial deletion of the short arm of chromosome 6;Swaay;Clin. Genet.,1988
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1. Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search;Molecular Cytogenetics;2021-07-24
2. 6p25 Interstitial deletion in two dizygotic twins with gyral pattern anomaly and speech and language disorder;European Journal of Paediatric Neurology;2013-05
3. Chromosome 6p25 Deletion Syndrome: Report of a case with optic disc coloboma and review of published ophthalmic findings;Ophthalmic Genetics;2012-04-12
4. Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders;Molecular Cytogenetics;2012-04-05
5. Schizophrenia in an adult with 6p25 deletion syndrome;American Journal of Medical Genetics Part A;2006
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