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
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61卷 / 04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：
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] Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two families
    J. Wang
    L. Spitz
    R. Hayward
    E. Kiely
    C. M. Hall
    D. P. O'Donoghue
    R. Palmer
    F. R. Goodman
    P. J. Scambler
    R. M. Winter
    W. Reardon
    European Journal of Pediatrics, 1999, 158 : 902 - 905
12345