CHROMOSOME SUBBAND 17P11.2 DELETION - A MINUTE DELETION SYNDROME

被引:33
作者
LOCKWOOD, D
HECHT, F
DOWMAN, C
HECHT, BK
RIZKALLAH, TH
GOODWIN, TM
ALLANSON, J
机构
[1] SW BIOMED RES INST,CTR GENET,6401 E THOMAS RD,TEMPE,AZ 85281
[2] MARICOPA MED CTR,DEPT OBSTET & GYNECOL,PHOENIX,AZ 85008
关键词
D O I
10.1136/jmg.25.11.732
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:732 / 737
页数:6
相关论文
共 11 条
  • [1] FAMILIAL MILLER-DIEKER SYNDROME ASSOCIATED WITH PERICENTRIC-INVERSION OF CHROMOSOME-17
    GREENBERG, F
    STRATTON, RF
    LOCKHART, LH
    ELDER, FFB
    DOBYNS, WB
    LEDBETTER, DH
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (04): : 853 - 859
  • [2] HITTNER HM, 1979, OPHTHALMOLOGY, V86, P1173
  • [3] CHROMOSOME-15 ANOMALIES AND THE PRADER-WILLI SYNDROME - CYTOGENETIC ANALYSIS
    MATTEI, MG
    SOUIAH, N
    MATTEI, JF
    [J]. HUMAN GENETICS, 1984, 66 (04) : 313 - 334
  • [4] INTERSTITIAL DELETION OF THE SHORT ARM OF CHROMOSOME-17
    PATIL, SR
    BARTLEY, JA
    [J]. HUMAN GENETICS, 1984, 67 (02) : 237 - 238
  • [5] INTERSTITIAL DELETION OF (17)(P11.2P11.2) IN 9 PATIENTS
    SMITH, ACM
    MCGAVRAN, L
    ROBINSON, J
    WALDSTEIN, G
    MACFARLANE, J
    ZONONA, J
    REISS, J
    LAHR, M
    ALLEN, L
    MAGENIS, E
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 24 (03): : 393 - 414
  • [6] INTERSTITIAL DELETION OF (17)(P11.2P11.2) - REPORT OF 6 ADDITIONAL PATIENTS WITH A NEW CHROMOSOME DELETION SYNDROME
    STRATTON, RF
    DOBYNS, WB
    GREENBERG, F
    DESANA, JB
    MOORE, C
    FIDONE, G
    RUNGE, GH
    FELDMAN, P
    SEKHON, GS
    PAULI, RM
    LEDBETTER, DH
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 24 (03): : 421 - 432
  • [7] FAMILIAL RETINOBLASTOMA AND CHROMOSOME-13 DELETION TRANSMITTED VIA AN INSERTIONAL TRANSLOCATION
    STRONG, LC
    RICCARDI, VM
    FERRELL, RE
    SPARKES, RS
    [J]. SCIENCE, 1981, 213 (4515) : 1501 - 1503
  • [8] HIGH-RESOLUTION OF HUMAN CHROMOSOMES
    YUNIS, JJ
    [J]. SCIENCE, 1976, 191 (4233) : 1268 - 1270
  • [9] 1987, CYTOGENET CELL GENET, V46, P357
  • [10] 1981, CYTOGENET CELL GENET, V31, P1