af Payeystie Kuhry Tins. I Am S Nghi, aee n
Nair V W F. Cysti diseases of tl kitney. In Bremner IM es The katoey
kaley disense. New Eng J Me+l. 1933.3291332-33
ny dissei PKI). PKDC and PKHDI. Curr (lpin Nrphming MH. Dvien KE, et aL. A highly polymorphie INA marker linked to adult gloyuy
polycystic kidney dfi
9. Wilson Pn Polycystin. Am Soc Ne
T Wu(. Hayashi T,et aL IKIE, u gene for pol kidney disease thnt
341 polycystie kidney disease. lichen Bioph
12. Wu (i Somo S Molecular geste and mechnism of autosomal dominant peolyrystir kidney isease(hy IM, Green WI. Lindsey JR, et aL. Germline and wrtie loss of function of the mouse epk14. Qian F, Watick Tl (hushi LF,et aL The moleular bsis of loveal ryst formatin in human maostdominant pol
5. Ia W.Fa aL Ia
16.w matic inactivation of IKIr results in polycystie kidney dlisease C'e1998.93:177-188 I7. Watnick T He N. Wame K,et al. Mutation of PKDl m ALNKDe cysts suggust n pathogenic effect olI. van Aaelshesg Is The ole of tl polyoystims in kidney developmen. Pediatr Nephrad 1999.L,
154459 G:l. Ackert H Vino Y, el aL Chlanyciononas IFT8R and its rmm hm siga, palysystr
lk. lo X The palyeyatir
ilen M A
\.et nt U
lo, Fidler T, schrier RW. Hyper
32. Foder T, Edelstein C, Fick Boshan GM,et al Progress in blood pressare contral in tusoswml dm
36. MogEsiDat R He N Wane K,e al. Cremmype retal fimm tin correlaton it iype 2 an
38. Ritx E, Zeier M. Waldherr R, P'Tegrssion Io wv. I: Watson ML. Torres VE es. Poly
理断基结水昌,落万学,超声医学,学3,北京;料学技木文量出期社
nltt paly..张树忠,则庆文,梅长林常染色体显性遗传性多囊肾病常用的基因诊断拉术中华病杂志,200
L. Iwwa ZH. tupu S, Warll CA tt nl. Pain maragement im il
New insights into polyeyatir kitty dimwit and its
H-f kate
ain F, Grunfeld JI. Li
ridley diseasVE Aitoeormal dorms polycystin kiring afeas. In heeran
oh. Pe
her Let al. Mapwinw of the gete for amsel receive golyeysn kidney
patir she I eta
e pale let helis I repeats Am J Hum Lenet2102.701112-1a1
I: Selleck t,nt aL m in the gene fer
kidey chinense (ARPKD)/ PKHD). I
Morula
4,:若85
Ww.Yug I,, Wilson F, et al. The autosomal recessive polycystie kit
El). Woychik RP, Dll KM.et aL Cellinr pathophysiology of cystic kidney disease
I Dv Biol.19,43:45746
71, Fonck doux MF, et al. Autosomal
hood, Nephrol Dhal T'mnsplanl, 2001, 16: 1148-1654
2. Thomas W). Shney S Siegel I M. Acute visual loss in u child with autosome polyeystic kid.
port and review t
73. Zerre K. Mather G. lecker J ,et aL Prenatal polycystic kidney disease
ARPKD), moleculr geneties,clincal nd fetal morphology. Am J Med Genet, 1996.76
74. Nicolau C, Torra R, Hlndenas C, et al. Sonographic patlerns of
范5,Pe C, et aL A
/4 Ken S crackI LI. Hildebrant Fet al.
imaging nnd RARE M
kilter
78. bosch 1M. Plank C Rascher W, et al. Autiontnl recessive polyeystic kidy diseas
162:43843979.T-inaraio M. Clore S,