WARSAW BREAKAGE SYNDROME: FURTHER CLINICAL AND GENETIC DELINEATION

被引：0

作者：

Alkhunaizi, E. ^{[1
,2
]}

Shaheen, R. ^{[3
]}

Bharti, S. K. ^{[4
]}

Joseph-George, A. M. ^{[5
]}

Chong, K. ^{[1
]}

Abdel-Salam, G. M. H. ^{[6
]}

Alowain, M. ^{[7
]}

Blaser, S. I. ^{[8
]}

Papsin, B. C. ^{[9
]}

Hashem, M. ^{[3
]}

Martin, N. ^{[1
]}

Godoy, R. ^{[1
]}

Brosh, R. M., Jr. ^{[4
]}

Alkuraya, F. S. ^{[3
,9
,10
]}

Chitayat, D. ^{[1
,2
]}

机构：

[1] Univ Toronto, Prenatal Diag & Med Genet Program, Mt Sinai Hosp, Dept Obstet & Gynecol, Toronto, ON, Canada

[2] Univ Toronto, Hosp Sick Children, Div Clin & Metab Genet, Dept Pediat, Toronto, ON, Canada

[3] King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh, Saudi Arabia

[4] NIA, Lab Mol Gerontol, NIH, Biomed Res Ctr, Baltimore, MD 21224 USA

[5] Univ Toronto, Hosp Sick Children, Dept Pediat Lab Med, Cytogen Lab,Div Genome Diagnost, Toronto, ON, Canada

[6] Natl Res Ctr, Human Genet & Genome Res Div, Dept Clin Genet, Cairo, Egypt

[7] King Faisal Specialist Hosp & Res Ctr, Dept Med Genet, Riyadh, Saudi Arabia

[8] Univ Toronto, Hosp Sick Children, Div Neuroradiol, Dept Diagnost Imaging, Toronto, ON, Canada

[9] Univ Toronto, Hosp Sick Children, Dept Otolaryngol Head & Neck Surg, Toronto, ON, Canada

[10] King Abdulaziz City Sci & Technol, Saudi Human Genome Program, King, WI, Saudi Arabia

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 2019年 / 179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：

引用

页码：715 / 715

页数：1

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