Further demonstration of phenotypic heterogeneity in chromosome 22q11.2 deletion.

被引：0
|
作者：
Medeiros, P
Gilgenkrantz, S
DeGeeter, B
Livolsi, A
Geraudel, A
Alembik, Y
Stoll, C
机构：
[1] CHU STRASBOURG,SERV GENET MED,F-67000 STRASBOURG,FRANCE
[2] CHU STRASBOURG,SERV PEDIAT,F-67000 STRASBOURG,FRANCE
[3] CTR TRANSFUS SANGUINE,LAB CYTOGENET,NANCY,FRANCE
来源：
CYTOGENETICS AND CELL GENETICS | 1997年 / 77卷 / 1-2期
关键词：
D O I：
暂无
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
引用
收藏
页码：P252 / P252
页数：1
相关论文
共 50 条
  • [1] The spectrum of the chromosome 22q11.2 deletion.
    McDonald-McGinn, DM
    LaRossa, D
    Randall, P
    Goldmuntz, E
    Clarke, BJ
    Sullivan, K
    Eicher, P
    Lynch, D
    Binghsm, P
    Wang, P
    Gerdes, M
    Moss, E
    Solot, C
    Moshang, T
    Ming, JE
    Driscoll, D
    Emanuel, BS
    Zackai, EH
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A106 - A106
  • [2] Guidelines for prenatal detection of the 22q11.2 deletion.
    McDonald-McGinn, DM
    Driscoll, DA
    Saitta, S
    Jawad, A
    Tonnesen, M
    Ming, JE
    Goldmuntz, E
    Canning, D
    Spinner, N
    Emanuel, BS
    Zackai, EH
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 198 - 198
  • [3] Neonatal respiratory death in the 22q11.2 deletion.
    Russell, KL
    McDonald-McGinn, DM
    Mahle, W
    Howell, L
    Kasperski, S
    Wilkes, BM
    Meyer-Cohen, J
    Adzick, S
    Zackai, EH
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A342 - A342
  • [4] The first autopsy series in patients with a 22q11.2 deletion.
    Huff, DS
    McDonald-McGinn, DM
    Zackai, EH
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 283 - 283
  • [5] The neurocognitive and psychosocial profile in children with a 22q11.2 deletion.
    Bearden, CE
    Woodin, M
    Moss, E
    Wang, P
    Driscoll, D
    Emanuel, BS
    McDonald-McGinn, DM
    Cannon, TD
    Zackai, EH
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A142 - A142
  • [6] A population-based study of the 22q11.2 deletion.
    Botto, LD
    Campbell, RM
    Coleman, K
    Correa, A
    Elixson, EM
    Erickson, JD
    Fernhoff, P
    May, K
    Merritt, R
    O'Leary, L
    Rasmussen, SA
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 283 - 283
  • [7] FAMILY STUDIES IN CHROMOSOME 22Q11 DELETION - FURTHER DEMONSTRATION OF PHENOTYPIC HETEROGENEITY
    DESILVA, D
    DUFFTY, P
    BOOTH, P
    AUCHTERLONIE, I
    MORRISON, N
    DEAN, JCS
    [J]. CLINICAL DYSMORPHOLOGY, 1995, 4 (04) : 294 - 303
  • [8] Psycho-educational characterization of patients with a 22Q11.2 deletion.
    Wang, PP
    Moss, E
    McDonaldMcGinn, DM
    Reed, LA
    Driscoll, DA
    Emanuel, BS
    Zackai, EH
    [J]. PEDIATRIC RESEARCH, 1996, 39 (04) : 878 - 878
  • [9] Parent of origin does not determine phenotype in the 22q11.2 deletion.
    McDonald-McGinn, DM
    Driscoll, DA
    Tonnesen, M
    Sullivan, K
    Kirschner, R
    Goldmuntz, E
    Weinzimer, S
    Lynch, D
    Wang, P
    Moss, E
    Gerdes, M
    Solot, C
    Catania, C
    Saitta, S
    Emanuel, BS
    Zackai, EH
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 285 - 285
  • [10] Genitourinary malformations in chromosome 22q11.2 deletion
    Wu, HY
    Rusnack, SL
    Bellah, RD
    Plachter, N
    McDonald-McGinn, DM
    Zackai, EH
    Canning, DA
    [J]. JOURNAL OF UROLOGY, 2002, 168 (06): : 2564 - 2565
12345