TY - JOUR AU - Quinonez, S. C. AU - Innis, J. W. PY - 2014 DA - 2014// TI - Human HOX gene disorders JO - Mol Genet Metab VL - 111 UR - https://doi.org/10.1016/j.ymgme.2013.10.012 DO - 10.1016/j.ymgme.2013.10.012 ID - Quinonez2014 ER - TY - JOUR AU - Di-Poï, N. AU - Koch, U. AU - Radtke, F. AU - Duboule, D. PY - 2010 DA - 2010// TI - Additive and global functions of HoxA cluster genes in mesoderm derivatives JO - Dev Biol VL - 341 UR - https://doi.org/10.1016/j.ydbio.2010.03.006 DO - 10.1016/j.ydbio.2010.03.006 ID - Di-Poï2010 ER - TY - JOUR AU - Jun, K. R. AU - Seo, E. J. AU - Lee, J. O. AU - Yoo, H. W. AU - Park, I. S. AU - Yoon, H. K. PY - 2011 DA - 2011// TI - Molecular cytogenetic and clinical characterization of a patient with a 5.6-Mb deletion in 7p15 including HOXA cluster JO - Am J Med Genet A VL - 155 UR - https://doi.org/10.1002/ajmg.a.33860 DO - 10.1002/ajmg.a.33860 ID - Jun2011 ER - TY - JOUR AU - Hosoki, K. AU - Ohta, T. AU - Fujita, K. AU - Nishigaki, S. AU - Shiomi, M. AU - Niikawa, N. PY - 2012 DA - 2012// TI - Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome JO - Pediatr Int VL - 54 UR - https://doi.org/10.1111/j.1442-200X.2011.03550.x DO - 10.1111/j.1442-200X.2011.03550.x ID - Hosoki2012 ER - TY - JOUR AU - Devriendt, K. AU - Jaeken, J. AU - Matthijs, G. AU - Esch, H. AU - Debeer, P. AU - Gewillig, M. PY - 1999 DA - 1999// TI - Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalli JO - Am J Hum Genet VL - 65 UR - https://doi.org/10.1086/302452 DO - 10.1086/302452 ID - Devriendt1999 ER - TY - JOUR AU - Dunø, M. AU - Hove, H. AU - Kirchhoff, M. AU - Devriendt, K. AU - Schwartz, M. PY - 2004 DA - 2004// TI - Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion JO - Hum Genet VL - 115 UR - https://doi.org/10.1007/s00439-004-1174-y DO - 10.1007/s00439-004-1174-y ID - Dunø2004 ER - TY - JOUR AU - Kosaki, R. AU - Higuchi, M. AU - Mitsui, N. AU - Matsushima, K. AU - Ohashi, H. AU - Kosaki, K. PY - 2005 DA - 2005// TI - Deletion involving the TWIST locus and the HOXA cluster: a contiguous gene syndrome on 7p? JO - Congenit Anom VL - 45 UR - https://doi.org/10.1111/j.1741-4520.2005.00059.x DO - 10.1111/j.1741-4520.2005.00059.x ID - Kosaki2005 ER - TY - JOUR AU - Fryssira, H. AU - Makrythanasis, P. AU - Kattamis, A. AU - Stokidis, K. AU - Menten, B. AU - Kosaki, K. PY - 2011 DA - 2011// TI - Severe Developmental Delay in a Patient with 7p21.1–p14.3 Microdeletion Spanning the TWIST Gene and the HOXA Gene Cluster JO - Mol Syndromol VL - 2 ID - Fryssira2011 ER - TY - JOUR AU - Hoover-Fong, J. E. AU - Cai, J. AU - Cargile, C. B. AU - Thomas, G. H. AU - Patel, A. AU - Griffin, C. A. PY - 2003 DA - 2003// TI - Facial dysgenesis: a novel facial syndrome with chromosome 7 deletion p 15.1–21.1 JO - Am J Med Genet A VL - 117 UR - https://doi.org/10.1002/ajmg.a.10046 DO - 10.1002/ajmg.a.10046 ID - Hoover-Fong2003 ER - TY - BOOK AU - Shaffer, L. G. AU - McGowan-Jordan, J. AU - Schmid, M. PY - 2013 DA - 2013// TI - ISCN (2013): An International system for human cytogenetic nomenclature PB - S. Karger CY - Basel ID - Shaffer2013 ER - TY - JOUR AU - Hastings, R. J. AU - Cavani, S. AU - Bricarelli, F. D. AU - Patsalis, P. C. AU - Kristoffersson, U. PY - 2007 DA - 2007// TI - Cytogenetic guidelines and quality assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations JO - Eur J Hum Genet VL - 15 UR - https://doi.org/10.1038/sj.ejhg.5201809 DO - 10.1038/sj.ejhg.5201809 ID - Hastings2007 ER - TY - JOUR AU - Hammerman, C. AU - Kaplan, M. PY - 1995 DA - 1995// TI - Oxygen saturation during and after feeding in healthy term infants JO - Biol Neonate VL - 67 UR - https://doi.org/10.1159/000244149 DO - 10.1159/000244149 ID - Hammerman1995 ER - TY - JOUR AU - Abu Jawdeh, E. G. AU - Martin, R. J. PY - 2013 DA - 2013// TI - Neonatal apnea and gastroesophageal reflux (GER): is there a problem? JO - Early Hum Dev VL - 89 UR - https://doi.org/10.1016/S0378-3782(13)70005-7 DO - 10.1016/S0378-3782(13)70005-7 ID - Abu Jawdeh2013 ER - TY - JOUR AU - Pal, B. R. AU - Preston, P. R. AU - Morgan, M. E. AU - Rushton, D. I. AU - Durbin, G. M. PY - 2001 DA - 2001// TI - Frontal horn thin walled cysts in preterm neonates are benign JO - Arch Dis Child Fetal Neonatal VL - 85 UR - https://doi.org/10.1136/fn.85.3.F187 DO - 10.1136/fn.85.3.F187 ID - Pal2001 ER - TY - JOUR AU - Aubin, J. AU - Lemieux, M. AU - Tremblay, M. AU - Bérard, J. AU - Jeannotte, L. PY - 1997 DA - 1997// TI - Early postnatal lethality in Hoxa-5 mutant mice is attributable to respiratory tract defects JO - Dev Biol VL - 192 UR - https://doi.org/10.1006/dbio.1997.8746 DO - 10.1006/dbio.1997.8746 ID - Aubin1997 ER - TY - JOUR AU - Chisaka, O. AU - Capecchi, M. R. PY - 1991 DA - 1991// TI - Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5 JO - Nature VL - 350 UR - https://doi.org/10.1038/350473a0 DO - 10.1038/350473a0 ID - Chisaka1991 ER - TY - JOUR AU - Manley, N. R. AU - Capecchi, M. R. PY - 1995 DA - 1995// TI - The role of Hoxa-3 in mouse thymus and thyroid development JO - Development VL - 121 ID - Manley1995 ER - TY - JOUR AU - Chojnowski, J. L. AU - Masuda, K. AU - Trau, H. A. AU - Thomas, K. AU - Capecchi, M. AU - Manley, N. R. PY - 2014 DA - 2014// TI - Multiple roles for HOXA3 in regulating thymus and parathyroid differentiation and morphogenesis in mouse JO - Development VL - 19 UR - https://doi.org/10.1242/dev.110833 DO - 10.1242/dev.110833 ID - Chojnowski2014 ER - TY - JOUR AU - Koontz, J. I. AU - Soreng, A. L. AU - Nucci, M. AU - Kuo, F. C. AU - Pauwels, P. AU - Berghe, H. PY - 2001 DA - 2001// TI - Frequent fusion of the JAZF1 and JJAZ1 genes in endometrial stromal tumors JO - Proc Natl Acad Sci U S A VL - 98 UR - https://doi.org/10.1073/pnas.101132598 DO - 10.1073/pnas.101132598 ID - Koontz2001 ER - TY - JOUR AU - Pangrazio, A. AU - Fasth, A. AU - Sbardellati, A. AU - Orchard, P. J. AU - Kasow, K. A. AU - Raza, J. PY - 2013 DA - 2013// TI - SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity JO - J Bone Miner Res VL - 28 UR - https://doi.org/10.1002/jbmr.1849 DO - 10.1002/jbmr.1849 ID - Pangrazio2013 ER - TY - JOUR AU - Lehoczky, J. A. AU - Williams, M. E. AU - Innis, J. W. PY - 2004 DA - 2004// TI - Conserved expression domains for genes upstream and within the HoxA and HoxD clusters suggests a long-range enhancer existed before cluster duplication JO - Evol Dev VL - 6 UR - https://doi.org/10.1111/j.1525-142X.2004.04050.x DO - 10.1111/j.1525-142X.2004.04050.x ID - Lehoczky2004 ER -