Sacral agenesis and holoprosencephaly associated with a submicroscopic 7q36 deletion.

被引:0
|
作者
Siu, VM
Belloni, E
Shi, XM
Tsui, LC
Scherer, SW
机构
[1] Univ Western Ontario, Dept Pediat, Div Med Genet, London, ON N6A 3K7, Canada
[2] CPRI, London, England
[3] Univ Toronto, Toronto, ON, Canada
[4] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
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
638
引用
收藏
页码:A113 / A113
页数:1
相关论文
共 50 条
  • [31] Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome
    Wouters, CH
    Meijers-Heijboer, HJ
    Eussen, BJFMM
    van der Heide, AA
    van Luijk, RB
    van Drunen, E
    Beverloo, BB
    Visscher, F
    Van Hemel, JO
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 102 (03): : 261 - 265
  • [32] Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report
    El Amrani, Zhour
    Natiq, Abdelhafid
    Sbiti, Aziza
    Ratbi, Ilham
    Liehr, Thomas
    Sefiani, Abdelaziz
    Sahli, Maryem
    MOLECULAR SYNDROMOLOGY, 2024, 15 (02) : 125 - 129
  • [33] Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene
    Linhares, Natalia D.
    Svartman, Marta
    Salgado, Mauro Ivan
    Rodrigues, Tatiane C.
    da Costa, Silvia S.
    Rosenberg, Carla
    Valadares, Eugenia R.
    META GENE, 2014, 2 : 16 - 24
  • [34] Identification and genetic analysis of pigmentary glaucoma loci on 7q36 and 18q
    Andersen, JS
    DelBono, EA
    Haines, JL
    Wiggs, JL
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1999, 40 (04) : S596 - S596
  • [35] A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36
    Heus, HC
    Hing, A
    van Baren, MJ
    Joose, M
    Breedveld, GJ
    Wang, JC
    Burgess, A
    Donnis-Keller, H
    Berglund, C
    Zguricas, J
    Scherer, SW
    Rommens, JM
    Oostra, BA
    Heutink, P
    GENOMICS, 1999, 57 (03) : 342 - 351
  • [36] Evidence for an additional susceptibility region for autism on human chromosome 7q36
    Huq, AHMM
    Zhong, HL
    Nabi, R
    Chugani, DC
    Serajee, FJ
    ANNALS OF NEUROLOGY, 2002, 52 (03) : S116 - S117
  • [37] A locus for preaxial polydactyly with sternal abnormalities maps to chromosome 7q36
    Gordon, T
    Dundar, M
    Cooke, A
    Ozyazgan, I
    Oguzkaya, F
    Ozkul, Y
    Holloway, S
    Tolmie, J
    Goodman, F
    JOURNAL OF MEDICAL GENETICS, 2000, 37 : S81 - S81
  • [38] A COMPLEX BILATERAL POLYSYNDACTYLY DISEASE LOCUS MAPS TO CHROMOSOME 7Q36
    TSUKUROV, O
    BOEHMER, A
    FLYNN, J
    NICOLAI, JP
    HAMEL, BCJ
    TRAILL, S
    ZALESKE, D
    MANKIN, HJ
    YEON, H
    HO, C
    TABIN, C
    SEIDMAN, JG
    SEIDMAN, C
    NATURE GENETICS, 1994, 6 (03) : 282 - 286
  • [39] Holoprosencephaly and cystic renal dysplasia associated with der(7)t(7;9)(q36;q32)mat.
    Risheg, H
    Seaver, L
    Lebel, R
    Srivastava, A
    Menon, S
    DuPont, B
    GENETICS IN MEDICINE, 2004, 6 (04) : 328 - 328
  • [40] A syndrome of multiple exostoses, hirsutism, mental retardation and seizures in a patient with a 8q24 submicroscopic interstitial deletion.
    Van Maldergem, L
    Wuyts, W
    Foulon, M
    Wetzburger, C
    Roland, D
    Gillerot, Y
    Van Hul, W
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A347 - A347