210 related articles for article (PubMed ID: 28422522)
1. Molecular Genetic Characterization of a Chinese Family with Severe Split Hand/Foot Malformation.
Cao L; Yang W; Wang S; Chen C; Zhang X; Luo Y
Genet Test Mol Biomarkers; 2017 Jun; 21(6):357-362. PubMed ID: 28422522
[TBL] [Abstract][Full Text] [Related]
2. [A DNA duplication at chromosome 10q24.3 is associated with split-hand split-foot malformation in a Chinese family].
Yang W; Hu ZJ; Yu XF; Li QH; Zhang AJ; Deng X; Zhang AY; Gao CS; Liu Y; Ao Y; Lo WH; Zhang X
Zhonghua Yi Xue Za Zhi; 2006 Mar; 86(10):652-8. PubMed ID: 16681918
[TBL] [Abstract][Full Text] [Related]
3. Microduplication of BTRC detected in a Chinese family with split hand/foot malformation type 3.
Qiu L; Li C; Zheng G; Yang T; Yang F
Clin Genet; 2022 Nov; 102(5):451-456. PubMed ID: 35908152
[TBL] [Abstract][Full Text] [Related]
4. [Genetic analysis of a pedigree affected with congenital split-hand/foot malformation].
Li Q; Tong M; Chen C; Ji Y; Zhou K; Xu G; Hu S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):467-470. PubMed ID: 32219839
[TBL] [Abstract][Full Text] [Related]
5. Discontinuous microduplications at chromosome 10q24.31 identified in a Chinese family with split hand and foot malformation.
Dai L; Deng Y; Li N; Xie L; Mao M; Zhu J
BMC Med Genet; 2013 Apr; 14():45. PubMed ID: 23596994
[TBL] [Abstract][Full Text] [Related]
6. Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation.
Everman DB; Morgan CT; Lyle R; Laughridge ME; Bamshad MJ; Clarkson KB; Colby R; Gurrieri F; Innes AM; Roberson J; Schrander-Stumpel C; van Bokhoven H; Antonarakis SE; Schwartz CE
Am J Med Genet A; 2006 Jul; 140(13):1375-83. PubMed ID: 16761290
[TBL] [Abstract][Full Text] [Related]
7. Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.
Kano H; Kurosawa K; Horii E; Ikegawa S; Yoshikawa H; Kurahashi H; Toda T
Hum Genet; 2005 Dec; 118(3-4):477-83. PubMed ID: 16235095
[TBL] [Abstract][Full Text] [Related]
8. Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements.
Dimitrov BI; de Ravel T; Van Driessche J; de Die-Smulders C; Toutain A; Vermeesch JR; Fryns JP; Devriendt K; Debeer P
J Med Genet; 2010 Feb; 47(2):103-11. PubMed ID: 19584065
[TBL] [Abstract][Full Text] [Related]
9. [Genetic analysis of three families affected with split-hand/split-foot malformation].
He W; Lin G; Liang P; Cheng D; Hu X; Zhou L; Xiong B; Tan Y; Lu G; Li W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):476-480. PubMed ID: 28777841
[TBL] [Abstract][Full Text] [Related]
10. [Identification of pathogenic mutation in a Chinese pedigree affected with split hand/split foot malformation].
Zhuo Z; Zhai Y; Jin P; Yan W; Kong H; Fang X; Li F; Luo Q; Kong X; Wang H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec; 35(6):808-811. PubMed ID: 30512151
[TBL] [Abstract][Full Text] [Related]
11. Microduplications of 10q24 Detected in Two Chinese Patients with Split-hand/foot Malformation Type 3.
Xiang R; Du R; Guo S; Jin JY; Fan LL; Tang JY; Zhou ZB
Ann Clin Lab Sci; 2017 Nov; 47(6):754-757. PubMed ID: 29263051
[TBL] [Abstract][Full Text] [Related]
12. Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region.
Lyle R; Radhakrishna U; Blouin JL; Gagos S; Everman DB; Gehrig C; Delozier-Blanchet C; Solanki JV; Patel UC; Nath SK; Gurrieri F; Neri G; Schwartz CE; Antonarakis SE
Am J Med Genet A; 2006 Jul; 140(13):1384-95. PubMed ID: 16691619
[TBL] [Abstract][Full Text] [Related]
13. [Identification of a pathogenic microduplication in a Chinese split-hand/split-foot malformation family].
Liu Y; Huang Y; Yang W; Zhang X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):276-9. PubMed ID: 24928001
[TBL] [Abstract][Full Text] [Related]
14. Split-hand/foot malformation 3 resulting from microduplications in 10q24 region in five patients from India.
Langeh N; Ansari MT; Kabra M; Gupta N
Am J Med Genet A; 2024 May; 194(5):e63520. PubMed ID: 38168117
[TBL] [Abstract][Full Text] [Related]
15. Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.
Ozen RS; Baysal BE; Devlin B; Farr JE; Gorry M; Ehrlich GD; Richard CW
Am J Hum Genet; 1999 Jun; 64(6):1646-54. PubMed ID: 10330351
[TBL] [Abstract][Full Text] [Related]
16. Molecular genetic characterization of a Korean split hand/split foot malformation (SHFM).
Kang YS; Cheong HM; Moon Y; Lee IB; Kim SM; Kim HS; Jun SY; Jung SK; Kim JS; Choi JH; Cho HE; Son JS; Min NY; Lee KH
Mol Cells; 2004 Jun; 17(3):397-403. PubMed ID: 15232212
[TBL] [Abstract][Full Text] [Related]
17. Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families.
Aziz A; Irfanullah ; Khan S; Zimri FK; Muhammad N; Rashid S; Ahmad W
Gene; 2014 Jan; 534(2):265-71. PubMed ID: 24211389
[TBL] [Abstract][Full Text] [Related]
18. [Congenital ectrodactyly caused by chromosome 10q24.31 duplication and its pathogenetic analysis].
Zhang XQ; Wang J; Xiong F; Lv WB; Zhou YQ; Yang SM; Zhang YT; Tian XY; Lian W; Xu XM
Yi Chuan; 2019 Aug; 41(8):716-724. PubMed ID: 31447422
[TBL] [Abstract][Full Text] [Related]
19. Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25.
Raas-Rothschild A; Manouvrier S; Gonzales M; Farriaux JP; Lyonnet S; Munnich A
J Med Genet; 1996 Dec; 33(12):996-1001. PubMed ID: 9004130
[TBL] [Abstract][Full Text] [Related]
20. A novel homozygous missense mutation in WNT10B in familial split-hand/foot malformation.
Khan S; Basit S; Zimri FK; Ali N; Ali G; Ansar M; Ahmad W
Clin Genet; 2012 Jul; 82(1):48-55. PubMed ID: 21554266
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
