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| X-linked Hypophosphatemic Rickets, del(2)(q37.1;q37.3) Deletion Syndrome and Mosaic Turner Syndrome, mos 45,X/46,X, del(2)(q37.1;q37.3) in a 3-year-old Female |
| Alaina P. Vidmar, Brian Miyazaki, Pedro A. Sanchez-Lara, Pisit Pitukcheewanont |
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jbm. 2017;24(4):257-261. Published online November 30, 2017 DOI: https://doi.org/10.11005/jbm.2017.24.4.257 |
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X-linked Hypophosphatemic Rickets, del(2)(q37.1;q37.3) Deletion Syndrome and Mosaic Turner Syndrome, mos 45,X/46,X, del(2)(q37.1;q37.3) in a 3-year-old Female Journal of Bone Metabolism. 2017;24(4):257  Deletion (2) (q37) American Journal of Medical Genetics. 1994;51(2):153-155 Terminal deletion of the long arm of chromosome 2 in a premature infant with karyotype: 46,XY,del(2)(q37) American Journal of Medical Genetics. 1994;49(4):399-401 Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37) American Journal of Medical Genetics. 1989;32(3):350-352 Translocation (2;11)(q37;q23) in therapy-related myelodysplastic syndrome after treatment for acute promyelocytic leukemia Cancer Genetics and Cytogenetics. 2008;180(2):149-152 Spindle-cell rhabdomyosarcoma with 2q36∼q37 involvement Cancer Genetics and Cytogenetics. 2003;140(1):62-65 Hornerin gene was involved in a case of acute myeloid leukemia transformed from myelodysplastic syndrome with t(1;2)(q21;q37) Leukemia. 2006;20(12):2184-2187 Assignment of the human glypican gene (GPC1) to 2q35–q37 by fluorescence in situ hybridization Genomics. 1995;25(1):327-329 Presence of three recurrent chromosomal rearrangements, t(2;3)(p12;q37), del(8)(q24), and t(14;18), in an acute lymphoblastic leukemia Cancer Genetics and Cytogenetics. 1996;86(1):76-79 Chromosome translocation (2;13) (q37;q14) in a disseminated alveolar rhabdomyosarcoma European Journal of Pediatrics. 1988;148(1):69-71 |
