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Search Results for - POTTER'S ANOMALY OF THE KIDNEY

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ID
 
Description
 
Product
 
Source
(Showing Items: 50)
 
 
 
 
RENAL ADYSPLASIA
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
RENAL ADYSPLASIA
 
Fibroblast
 
 
 
 
 
ROKITANSKY-KUSTER-HAUSER SYNDROME | RENAL ADYSPLASIA
 
DNA
 
LCL
 
 
 
 
ROKITANSKY-KUSTER-HAUSER SYNDROME | RENAL ADYSPLASIA
 
LCL
 
B-Lymphocyte
 
 
 
 
ROKITANSKY-KUSTER-HAUSER SYNDROME
 
LCL
 
B-Lymphocyte
 
 
 
 
ROKITANSKY-KUSTER-HAUSER SYNDROME
 
DNA
 
LCL
 
 
 
 
VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD
 
DNA
 
LCL
 
 
 
 
VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD
 
LCL
 
B-Lymphocyte
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1
 
DNA
 
LCL
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1
 
Fibroblast
 
Skin, Arm
 
 
 
 
CONGENITAL DISORDER OF DEGLYCOSYLATION; CDDG | N-GLYCANASE 1; NGLY1
 
LCL
 
B-Lymphocyte
 
 
 
 
TRANSLOCATED CHROMOSOME
 
LCL
 
B-Lymphocyte
 
 
 
 
SMITH-MAGENIS SYNDROME; SMS
 
LCL
 
B-Lymphocyte
 
 
 
 
FAMILIAL MULTIPLE CONGENITAL ANOMALIES - UNKNOWN SYNDROME OR INHERITANCE
 
Fibroblast
 
 
 
 
 
FRAGILE X MENTAL RETARDATION SYNDROME | FMR1 GENE; FMR1
 
Fibroblast
 
Kidney, Kidney
 
 
 
 
MUS
 
Kidney-derived cell line
 
Kidney
 
 
 
 
TRANSLOCATED CHROMOSOME
 
Amniotic fluid-derived cell line
 
Amniotic fluid
 
 
 
 
TRANSLOCATED CHROMOSOME
 
DNA
 
Amniotic fluid-derived cell line
 
 
 
 
POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1
 
Fibroblast
 
Kidney, Kidney
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
Fetal, Unspecified
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
CHROMOSOME DELETION
 
Fibroblast
 
 
 
 
 
CHROMOSOME DELETION
 
DNA
 
Fibroblast
 
 
 
 
POLYCYSTIC KIDNEYS
 
LCL
 
B-Lymphocyte
 
 
 
 
POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1
 
Fibroblast
 
 
 
 
 
POLYCYSTIC KIDNEYS
 
LCL
 
B-Lymphocyte
 
 
 
 
POLYCYSTIC KIDNEYS
 
LCL
 
B-Lymphocyte
 
 
 
 
PERSONAL GENOME PROJECT
 
DNA
 
LCL
 
 
 
 
PERSONAL GENOME PROJECT
 
LCL
 
B-Lymphocyte
 
 
 
 
PERSONAL GENOME PROJECT
 
High Molecular Weight DNA
 
B-Lymphocyte
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
Fibroblast
 
 
 
 
 
POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; PKHD1
 
Fibroblast
 
Skin, Unspecified
 
 
 
 
DIGEORGE SYNDROME; DGS
 
DNA
 
Fibroblast
 
 
 
 
DIGEORGE SYNDROME; DGS
 
Fibroblast
 
 
 
 
 
DIGEORGE SYNDROME; DGS
 
DNA
 
Fibroblast
 
 
 
 
DIGEORGE SYNDROME; DGS
 
Fibroblast
 
 
 
 
 
PERSONAL GENOME PROJECT
 
iPSC
 
B-Lymphocyte
 
 
 
 
POLYCYSTIC KIDNEYS
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPOPHOSPHATASIA, INFANTILE | ALKALINE PHOSPHATASE, LIVER; ALPL
 
Fibroblast
 
 
 
 
 
HYPOPHOSPHATASIA, INFANTILE | ALKALINE PHOSPHATASE, LIVER; ALPL
 
Fibroblast
 
 
 
 
 
NIA AGING CELL REPOSITORY'S LONGEVITY RESEARCH PROGRAM
 
LCL
 
B-Lymphocyte
 
 
 
 
NIA AGING CELL REPOSITORY'S LONGEVITY RESEARCH PROGRAM
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
LCL
 
B-Lymphocyte
 
 
 
 
HYPOPHOSPHATASIA; PHOSPHOETHANOLAMINURIA - 241500 OR 241510
 
LCL
 
B-Lymphocyte
 
 
 
 
DIGEORGE SYNDROME; DGS | TRANSLOCATED CHROMOSOME
 
DNA
 
Fibroblast
 
 
 
 
DIGEORGE SYNDROME; DGS | TRANSLOCATED CHROMOSOME
 
Fibroblast
 
 
 
 
 
PERSONAL GENOME PROJECT
 
LCL
 
B-Lymphocyte

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