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Volumn 56, Issue 3, 2001, Pages 181-192
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DNA diagnosis in hereditary nephropathies
a
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Author keywords
Chromosomal localization; Gene defect; Hereditary nephropathies; Heterogeneity
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Indexed keywords
DNA;
ALPORT SYNDROME;
BARTTER SYNDROME;
CYSTINOSIS;
DIAGNOSTIC PROCEDURE;
DISEASE CLASSIFICATION;
DNA DETERMINATION;
GENETIC DISORDER;
GENETIC HETEROGENEITY;
HETEROZYGOSITY;
HUMAN;
KIDNEY DISEASE;
KIDNEY POLYCYSTIC DISEASE;
KIDNEY TUMOR;
MEDULLARY SPONGE KIDNEY;
NEPHROGENIC DIABETES INSIPIDUS;
NEPHROLITHIASIS;
NEPHRONOPHTHISIS;
NEPHROTIC SYNDROME;
NOCTURNAL ENURESIS;
PATHOGENESIS;
PRENATAL DIAGNOSIS;
REVIEW;
CHROMOSOME MAPPING;
CYTOGENETIC ANALYSIS;
GENETIC COUNSELING;
GENETIC HETEROGENEITY;
GENETIC MARKERS;
GENETIC SCREENING;
HETEROZYGOTE DETECTION;
HUMANS;
KIDNEY DISEASES;
MUTATION;
PEDIGREE;
PRENATAL DIAGNOSIS;
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EID: 0034839764
PISSN: 03010430
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (3)
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References (6)
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