Genotype/phenotype correlations in split hand foot malformation (SHFM)

被引：0
|
作者：
Elliott, AM
Reed, MH
Evans, JA
机构：
[1] Univ Manitoba, Dept Biochem & Med Genet, Winnipeg, MB, Canada
[2] Childrens Hosp, Dept Radiol, Winnipeg, MB R3A 1S1, Canada
[3] Childrens Hosp, Dept Pediat & Child Hlth, Winnipeg, MB R3A 1S1, Canada
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 73卷 / 05期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
686
引用
收藏
页码：287 / 287
页数：1
相关论文
共 50 条
  • [1] Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients
    Elliott, Alison M.
    Evans, Jane A.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (13) : 1419 - 1427
  • [2] Split hand foot malformation (SHFM)
    Elliott, AM
    Evans, JA
    Chudley, AE
    CLINICAL GENETICS, 2005, 68 (06) : 501 - 505
  • [3] Split hand foot malformation (SHFM): An introduction
    Shanske, AL
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (13) : 1357 - 1358
  • [4] 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, AS
    Min, NY
    Lee, KH
    MOLECULES AND CELLS, 2004, 17 (03) : 397 - 403
  • [5] The association of split hand foot malformation (SHFM) and congenital heart defects
    Elliott, Alison M.
    Evans, Jane A.
    BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2008, 82 (06) : 425 - 434
  • [6] A rare complex malformation of the hand in split hand foot malformation type 3 (SHFM3)
    Ockeloen, Charlotte W.
    Cobben, Jan M.
    Marcelis, Carlo L. M.
    Koolen, David A.
    CLINICAL DYSMORPHOLOGY, 2013, 22 (03) : 106 - 108
  • [7] A search for causative genes of split hand/foot malformation (SHFM3).
    Kano, H
    Kurahashi, H
    Toda, T
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 321 - 321
  • [8] Classifications of split hand foot malformation (SHFM) should include transverse deficiencies: Why Maisels was correct
    Elliott, Alison M.
    Scott, William J., Jr.
    Chudley, Albert E.
    Reed, Martin H.
    Evans, Jane A.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2021, 185 (09) : 2809 - 2814
  • [9] Microduplication at 10q24 causing Split Hand Foot Malformation (SHFM) in an extensive pedigree
    Harrison, Victoria
    Williams, R.
    Connell, L.
    Kini, U.
    Blair, E.
    JOURNAL OF MEDICAL GENETICS, 2010, 47 : S48 - S48
  • [10] Mutation screening of the split hand foot malformation (SHFM3) by positional transcript analysis.
    Basel, D
    Homfrey, T
    Kilpatrick, MW
    Tsipouras, P
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 443 - 443
12345