Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas‐type polysyndactyly and Laurin‐Sandrow syndrome
暂无分享,去创建一个
S. Mundlos | M. Spielmann | E. Klopocki | S. Doelken | K. Girisha | K. Kjaer | M. Wajid | S. Patil | R. Floettmann | S. Lohan | R. Habenicht | W. Hülsemann | H. Abarca-Barriga | S. M. Baig | K. Girisha | F. Muhammad | S.C. Doelken | Ricarda Flöttmann | Stefan Mundlos | Muhammad Wajid | Silke Lohan | Shahid Mahmood Baig | Faqir Muhammad | Hugo Abarca-Barriga
[1] Yun Bai,et al. Confirmation of genetic homogeneity of syndactyly type IV and triphalangeal thumb–polysyndactyly syndrome in a Chinese family and review of the literature , 2013, European Journal of Pediatrics.
[2] M. Spielmann,et al. CNVs of noncoding cis-regulatory elements in human disease. , 2013, Current opinion in genetics & development.
[3] S. Mundlos,et al. Structural variations, the regulatory landscape of the genome and their alteration in human disease. , 2013, BioEssays : news and reviews in molecular, cellular and developmental biology.
[4] P. Robinson,et al. Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus. , 2012, American journal of human genetics.
[5] L. Lettice,et al. Human limb abnormalities caused by disruption of hedgehog signaling. , 2012, Trends in genetics : TIG.
[6] Abdelkader Essafi,et al. Opposing Functions of the ETS Factor Family Define Shh Spatial Expression in Limb Buds and Underlie Polydactyly , 2012, Developmental cell.
[7] S. Mundlos,et al. Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly , 2012, European Journal of Human Genetics.
[8] Harris Morrison,et al. Enhancer‐adoption as a mechanism of human developmental disease , 2011, Human mutation.
[9] S. Mundlos,et al. Copy-number variations, noncoding sequences, and human phenotypes. , 2011, Annual review of genomics and human genetics.
[10] S. Mundlos,et al. Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis. , 2011, American journal of human genetics.
[11] D. Wieczorek,et al. A specific mutation in the distant sonic hedgehog (SHH) cis‐regulator (ZRS) causes Werner mesomelic syndrome (WMS) while complete ZRS duplications underlie Haas type polysyndactyly and preaxial polydactyly (PPD) with or without triphalangeal thumb , 2010, Human mutation.
[12] S. Mundlos,et al. Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia , 2009, Nature Genetics.
[13] S. Mundlos,et al. Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2. , 2009, American journal of human genetics.
[14] Daisuke Sato,et al. A ZRS duplication causes syndactyly type IV with tibial hypoplasia , 2009, American journal of medical genetics. Part A.
[15] Z.-F. Zhang,et al. Triphalangeal thumb–polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancer , 2008, Journal of Medical Genetics.
[16] S. Mundlos,et al. A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome , 2008, Journal of Medical Genetics.
[17] J. Opitz,et al. Male‐to‐male transmission in Laurin–Sandrow syndrome and exclusion of RARB and RARG , 2005, American journal of medical genetics. Part A.
[18] M. Hosoya,et al. Elimination of a long-range cis-regulatory module causes complete loss of limb-specific Shh expression and truncation of the mouse limb , 2005, Development.
[19] B. Oostra,et al. A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly. , 2003, Human molecular genetics.
[20] J. Drouin,et al. Pitx1 and Pitx2 are required for development of hindlimb buds , 2003, Development.
[21] P. Kantaputra. Laurin-Sandrow syndrome with additional associated manifestations. , 2001, American journal of medical genetics.
[22] H. Steel,et al. Hereditary ulnar and fibular dimelia with peculiar facies. A case report. , 1970, The Journal of bone and joint surgery. American volume.
[23] C. Laurin,et al. BILATERAL ABSENCE OF THE RADIUS AND TIBIA WITH BILATERAL REDUPLICATION OF THE ULNA AND FIBULA. A CASE REPORT. , 1964, The Journal of bone and joint surgery. American volume.