The spectrum of the chromosome 22q11.2 deletion.

被引：0

作者：

McDonald-McGinn, DM ^{[1
]}

LaRossa, D ^{[1
]}

Randall, P ^{[1
]}

Goldmuntz, E ^{[1
]}

Clarke, BJ ^{[1
]}

Sullivan, K ^{[1
]}

Eicher, P ^{[1
]}

Lynch, D ^{[1
]}

Binghsm, P ^{[1
]}

Wang, P ^{[1
]}

Gerdes, M ^{[1
]}

Moss, E ^{[1
]}

Solot, C ^{[1
]}

Moshang, T ^{[1
]}

Ming, JE ^{[1
]}

Driscoll, D ^{[1
]}

Emanuel, BS ^{[1
]}

Zackai, EH ^{[1
]}

机构：

[1] Univ Penn, Childrens Hosp Philadelphia, Sch Med, Philadelphia, PA 19104 USA

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：

597

引用

页码：A106 / A106

页数：1

共 50 条

[1] Further demonstration of phenotypic heterogeneity in chromosome 22q11.2 deletion.
Medeiros, P
Gilgenkrantz, S
DeGeeter, B
Livolsi, A
Geraudel, A
Alembik, Y
Stoll, C
[J]. CYTOGENETICS AND CELL GENETICS, 1997, 77 (1-2): : P252 - P252
[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] 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
[8] 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
[9] 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
[10] Defining the clinical spectrum of deletion 22q11.2
Robin, NH
Shprintzen, RJ
[J]. JOURNAL OF PEDIATRICS, 2005, 147 (01): : 90 - 96

← 1 2 3 4 5 →