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PKHD1
LE WE PMID CA
PKHD113982PKHD1

Acrorenal field (Development)

Bardet Biedl syndrome

Caroli s syndrome

Caudal regression syndrome

Cloaca (Exstrophy)

Fetal Warfarin Syndrome

Hand and Wrist (Malformation)

Hydrolethalus Syndrome

Hypergammaglobulinemia idiopathic

Hyperglobulinemic purpura

IgM Nephropathy

Ivemark s syndrome

Kidney (Agenesis)

Kidney (C3NEF)

Kidney (Medullary cystic disease)

Kidney (Medullary sponge kidney)

Kidney (Radiation nephritis)

Kidney (Tip lesion)

Muckle Wells syndrome

Pallister Hall Syndrome

PCD (Heavy chain disease)

PKHD1

Poland s anomaly

Polytopic acrorenal developmental field defect

Potter s sequence

Radius (Aplasia)

Robinson s defect

Syndactyly

TTC8

Urinary blader (Megacystis)

Urinary tract (Obstructive uropathy)

2011  
1
Chiral separation by enantioselective liquid-liquid extraction.
[21107491] Org Biomol Chem 9(1): 36-51 (2011)
PMC   
2
Whole exome sequencing identifies recessive PKHD1 mutations in a Chinese twin family with Caroli disease.
[24710345] PLoS One 9(4):e92661 (2014)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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