[Potter's syndrome and polycystic kidney in the newborn].
作者信息
Pasquier B, Couderc P, Bost M, Rambaud P
出版信息
Sem Hop. 1971 Dec 8;47(49):2779-88.
PMID:4335740
Abstract
摘要
相似文献
1
[Potter's syndrome and polycystic kidney in the newborn].[新生儿波特综合征与多囊肾]
Sem Hop. 1971 Dec 8;47(49):2779-88.
2
[Potter syndrome (kidney agenesis) with chromosome abnormalities in the patient and mosaicism in the father].[患者患有波特综合征（肾缺如）且伴有染色体异常，父亲存在嵌合体现象]
Helv Paediatr Acta. 1971 Jun;26(2):210-4.
3
[Potter's syndrome with caudal appendix and feminine pseudohermaphroditism].[伴有尾状附件和女性假两性畸形的波特综合征]
Pediatrie. 1971 Sep;26(6):649-54.
4
Oligohydramnios sequence (Potter's syndrome): case clustering in northeastern Tennessee.羊水过少序列征（波特综合征）：田纳西州东北部的病例聚集情况
South Med J. 1987 May;80(5):585-92.
5
Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.梅克尔综合征一例的染色体异常（46,XX,3p 三体）
Birth Defects Orig Artic Ser. 1974;10(8):19-25.
6
[Ocular manifestations of trisomy 18].[18三体综合征的眼部表现]
Arch Ophtalmol Rev Gen Ophtalmol. 1972 Jun-Jul;32(6):457-76.
7
[Sirenomelia and multicystic renal dysplasia. Apropos of 2 cases].[并腿畸形与多囊性肾发育不良。附2例报告]
J Genet Hum. 1983 Dec;31 Suppl 5:403-11.
8
[Chromosome mosaic with 2 aneuploid stem lines in the tissue culture of a patient with multiple abnormalities].[一名患有多种异常的患者组织培养中存在含2个非整倍体干细胞系的染色体嵌合体]
Helv Paediatr Acta. 1966 Apr;21(1):72-84.
9
[Prenatal diagnosis of Potter's syndrome].[波特综合征的产前诊断]
Orv Hetil. 1984 Feb 19;125(8):457-60.
10
[Trisomy 18].[18三体综合征]
Nouv Presse Med. 1972 Mar 11;1(11):745-8.
引用本文的文献
1
Bilateral absence of the kidneys and ureters. Three cases reported in one family.双侧肾及输尿管缺如。一个家族中报告了3例。
J Med Genet. 1977 Jun;14(3):205-9. doi: 10.1136/jmg.14.3.205.
Zotero 插件