Further delineation of the 7q36 terminal deletion syndrome.

被引:0
|
作者
Kwan, A
Cherry, AM
Galperin, I
Huhn, S
Enns, GM
机构
[1] Stanford Univ, Sch Med, Div Med Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Div Cytogenet, Stanford, CA USA
[3] Stanford Univ, Sch Med, Div Neurosurg, Stanford, CA USA
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
619
引用
收藏
页码:289 / 289
页数:1
相关论文
共 50 条
  • [31] Genetic susceptibility to pre-eclampsia and chromosome 7q36
    Guo G.
    Lade J.A.
    Wilton A.N.
    Moses E.K.
    Grehan M.
    Fu Y.
    Qiu H.
    Cooper D.W.
    Brennecke S.P.
    Human Genetics, 1999, 105 (6) : 641 - 647
  • [32] Genetic susceptibility to pre-eclampsia and chromosome 7q36
    Guo, GL
    Lade, JA
    Wilton, AN
    Moses, EK
    Grehan, M
    Fu, YL
    Qiu, HY
    Cooper, DW
    Brennecke, SP
    HUMAN GENETICS, 1999, 105 (06) : 641 - 647
  • [33] Holoprosencephaly and familial translocations involving critical region 7q36
    Freund, M
    Bettesworth, N
    Hubinont, C
    Bernard, P
    Verellen, C
    CYTOGENETICS AND CELL GENETICS, 1999, 85 (1-2): : 148 - 148
  • [34] De novo 4q22 deletion: Report of two patients and delineation of clinical syndrome.
    Nowaczyk, MJM
    Teshima, IE
    SiegelBartelt, J
    Clarke, JTR
    PEDIATRIC RESEARCH, 1996, 39 (04) : 482 - 482
  • [35] LINKAGE OF PREAXIAL POLYDACTYLY TYPE-2 TO 7Q36
    HING, AV
    HELMS, C
    SLAUGH, R
    BURGESS, A
    WANG, JC
    HERMAN, T
    DOWTON, SB
    DONISKELLER, H
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 58 (02): : 128 - 135
  • [36] Further delineation of the Hennekam syndrome: A unique autosomal recessive lymphedema syndrome.
    Storm, AL
    Schelley, SL
    Hoyme, HE
    JOURNAL OF INVESTIGATIVE MEDICINE, 1999, 47 (02) : 56A - 56A
  • [37] Confirmation of 6q21-6q22.1 Deletion in Acro-Cardio-Facial Syndrome and Further Delineation of This Contiguous Gene Deletion Syndrome
    Hudson, Cindy
    Schwanke, Corbin
    Johnson, John P.
    Elias, Abdallah F.
    Phillips, Sandy
    Schwalbe, Tammy
    Tunby, Mary
    Xu, Dongbin
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (08) : 2109 - 2113
  • [38] HOLOPROSENCEPHALY AND SACRAL AGENESIS IN A FETUS WITH A TERMINAL DELETION 7Q36-]7QTER
    MORICHONDELVALLEZ, N
    DELEZOIDE, AL
    VEKEMANS, M
    JOURNAL OF MEDICAL GENETICS, 1993, 30 (06) : 521 - 524
  • [39] The further delineation of 6q and 7q subtelomeric deletion phenotype: natural histories and review of the literature
    Krajewska-Walasek, M.
    Gutkowska, A.
    Spodar, K.
    Marczak, A.
    Gajdulewicz, M.
    Jezela-Stanek, A.
    Chrzanowska, K. H.
    CHROMOSOME RESEARCH, 2007, 15 : 25 - 26
  • [40] LINKAGE OF A GENE CAUSING FAMILIAL HOLOPROSENCEPHALY (HPE) TO CHROMOSOME 7Q36
    MUENKE, M
    GURRIERI, F
    YI, D
    BAY, C
    COLLINS, AL
    JOHNSON, VP
    HENNEKAM, RCM
    SCHAEFER, GB
    LUBINSKY, MS
    MOORE, CA
    DOBYNS, WB
    MURRAY, JC
    PRICE, RA
    CYTOGENETICS AND CELL GENETICS, 1994, 65 (1-2): : 70 - 71