THE FRAGILE SITE ON CHROMOSOME-16-(Q21Q22) - DATA ON 4 NEW FAMILIES

被引：31
|
作者：
SHABTAI, F [1 ]
BICHACHO, S [1 ]
HALBRECHT, I [1 ]
机构：
[1] TEL AVIV UNIV,SACKLER SCH MED,RAMAT AVIV,ISRAEL
来源：
HUMAN GENETICS | 1980年 / 55卷 / 01期
关键词：
D O I：
10.1007/BF00329121
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：19 / 22
页数：4
相关论文
共 50 条
  • [21] Linkage analysis of schizophrenia to chromosome 1q21-22 in Taiwanese families
    Liu, CM
    Hwu, HG
    Ou-Yang, WC
    Lee, SFC
    Fann, CSJ
    Chu, CH
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (07): : 597 - 597
  • [22] LOCATION OF FRAGILE SITE - 16Q22.00
    MAGENIS, E
    CHAMBERLIN, J
    CYTOGENETICS AND CELL GENETICS, 1979, 25 (1-4): : 180 - 180
  • [23] INTERSTITIAL DELETION OF CHROMOSOME-16Q - 16Q22 IS CRITICAL FOR 16Q-SYNDROME
    FUJIWARA, M
    YOSHIMOTO, T
    MORITA, Y
    KAMADA, M
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (03): : 561 - 564
  • [24] ACUTE MYELOMONOCYTIC LEUKEMIA WITH MARROW EOSINOPHILIA (M4EO) AND INV(16)(P13Q22) IN A PATIENT WITH A HERITABLE FRAGILE SITE 16Q22
    ARTHUR, DC
    AASENG, SM
    BLOOMFIELD, CD
    CYTOGENETICS AND CELL GENETICS, 1985, 40 (1-4): : 572 - 572
  • [25] FAMILIAL FRAGILE SITE FOUND AT THE CANCER BREAKPOINT (1)(Q32) - INDUCIBILITY BY DISTAMYCIN-A, CONCOMITANCE WITH FRAGILE (16)(Q22)
    SHABTAI, F
    HART, J
    KLAR, D
    HALBRECHT, I
    HUMAN GENETICS, 1986, 73 (03) : 232 - 234
  • [26] Brachydactyly and short stature in a mother and her daughter with a fragile site at 16q22
    Stoll, C
    RoyDoray, B
    Dott, B
    Alembik, Y
    GENETIC COUNSELING, 1997, 8 (02): : 115 - 120
  • [27] FRAGILE SITE AT 4Q34
    DEWAN, K
    BORGAONKAR, DS
    REVISTA BRASILEIRA DE GENETICA, 1992, 15 (03): : 723 - 724
  • [28] A NEW INTERSTITIAL DELETION OF CHROMOSOME-4 DEL(4) (Q22-Q25)
    BUTLER, LJ
    PALMER, AV
    SPENCER, T
    TABIOSBROADWAY, R
    WALL, WJ
    CLINICAL GENETICS, 1987, 31 (04) : 199 - 205
  • [29] BEHAVIOR OF CHROMOSOME CORES AT HERITABLE FRAGILE SITES - 16Q22 AND XQ27
    HOWARDPEEBLES, PN
    HOWELL, WM
    CYTOGENETICS AND CELL GENETICS, 1981, 31 (02): : 115 - 119
  • [30] FAMILIAL FRAGILE SITE AT 16Q22 ASCERTAINED IN A NEWBORN WITH MAJOR BIRTH-DEFECTS
    DUNNER, JA
    MARTIN, AO
    TRAISMAN, HS
    TRAISMAN, ES
    ELIAS, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 1982, 34 (06) : A124 - A124
12345