343 related articles for article (PubMed ID: 4585577)
21. [Nail-patella syndrome: clinico-pathologic characteristics].
Trinn C; Szöke B; Magyarlaki T; Turi S; Ormos J; Nagy J
Orv Hetil; 1996 Oct; 137(41):2253-6. PubMed ID: 8992423
[TBL] [Abstract][Full Text] [Related]
22. Hereditary disorders of the kidney. I. Parenchymal defects and malformations.
Bernstein J; Kissane JM
Perspect Pediatr Pathol; 1973; 1():117-46. PubMed ID: 4596310
[No Abstract] [Full Text] [Related]
23. [Congenital and hereditary nephropathies in children based on epidemiological research data].
Ignatova MS; Fokeeva VV; Kalinina AA; Vel'tishchev IuE; Schuler D
Vestn Akad Med Nauk SSSR; 1984; (7):82-8. PubMed ID: 6236634
[No Abstract] [Full Text] [Related]
24. [Developmental anomalies and hereditary diseases of the kidney in ambulatory practice].
Smiljanić S; Kalinić-Andrić V; Jovanović D
Srp Arh Celok Lek; 1985 Sep; 113(9):763-7. PubMed ID: 3832468
[No Abstract] [Full Text] [Related]
25. [Comparative pathology of trisomies D and E].
Bocquet L
Union Med Can; 1968 Jul; 97(7):907-23. PubMed ID: 5709533
[No Abstract] [Full Text] [Related]
26. Cystic diseases of the kidney in children.
Landing BH; Gwinn JL; Lieberman E
Perspect Nephrol Hypertens; 1976; 4():187-200. PubMed ID: 177943
[TBL] [Abstract][Full Text] [Related]
27. Inherited renal disease and genetic counseling.
Kaplan MR
Clin Exp Dial Apheresis; 1981; 5(1-2):213-34. PubMed ID: 6277538
[TBL] [Abstract][Full Text] [Related]
28. [Congenital nephropathies].
Guignard JP
Rev Med Suisse Romande; 2000 Mar; 120(3):227-31. PubMed ID: 10815454
[TBL] [Abstract][Full Text] [Related]
29. Renal cysts in premature children: occurrence in a family with polycystic kidney disease.
Eulderink F; Hogewind BL
Arch Pathol Lab Med; 1978 Nov; 102(11):592-5. PubMed ID: 581452
[TBL] [Abstract][Full Text] [Related]
30. Monosomy 11q: report of two familial cases and review of the literature.
Hustinx R; Verloes A; Grattagliano B; Herens C; Jamar M; Soyeur D; Schaaps JP; Koulischer L
Am J Med Genet; 1993 Sep; 47(3):312-7. PubMed ID: 8135272
[TBL] [Abstract][Full Text] [Related]
31. Prevalence, phenotypic heterogeneity and familial aspects of bilateral renal agenesis/dysgenesis.
Holmes LB
Prog Clin Biol Res; 1989; 305():1-11. PubMed ID: 2762345
[No Abstract] [Full Text] [Related]
32. [Malformation syndrome and urinary organs].
Schönenberg H
Z Urol Nephrol; 1971 Jan; 64(1):61-73. PubMed ID: 5124718
[No Abstract] [Full Text] [Related]
33. [Malformation uropathies and multiple malformation syndromes].
Briard ML; Le Merrer M; Kaplan J; Bois E; Frézal J
J Genet Hum; 1984 Jun; 32(2):83-90. PubMed ID: 6736939
[TBL] [Abstract][Full Text] [Related]
34. Natural history of the recombinant (8) syndrome.
Sujansky E; Smith AC; Prescott KE; Freehauf CL; Clericuzio C; Robinson A
Am J Med Genet; 1993 Sep; 47(4):512-25. PubMed ID: 8256815
[TBL] [Abstract][Full Text] [Related]
35. [A rare case of a combination of hereditary amyloidosis and sarcoidosis].
Androsova SS; Kornev BM; Miroshnichenko NG; Privezentseva ND
Ter Arkh; 1995; 67(5):83-4. PubMed ID: 7638791
[No Abstract] [Full Text] [Related]
36. [Polycystic kidney disorders, genetic counseling and prenatal diagnosis].
Steffelaar JW; van Collenburg JJ; Niermeyer MF
Ned Tijdschr Geneeskd; 1980 Dec; 124(49):2073-9. PubMed ID: 7442848
[No Abstract] [Full Text] [Related]
37. [A child with Zellweger's cerebrohepatorenal syndrome].
Govaerts L; Corstiaensen J; Bakkeren J; Trujbels F; Monnens L
Tijdschr Kindergeneeskd; 1983 Apr; 51(2):65-7. PubMed ID: 6879587
[TBL] [Abstract][Full Text] [Related]
38. A high incidence of PKD in a large geographic area of south-western Hungary: a medical genetic study.
Forrai G; Tauszik T; Tauszik N; Mohr T; Tunyogi MC; Holics C; Bánkövi G; Gál I
Prog Clin Biol Res; 1989; 305():89-94. PubMed ID: 2762359
[No Abstract] [Full Text] [Related]
39. [Alport's syndrome (heredo-familial glomerulonephritis with deafness and eye abnormalities)].
Genova R
Clin Pediatr (Bologna); 1971 Sep; 53(9):301-13. PubMed ID: 5004353
[No Abstract] [Full Text] [Related]
40. Del(15)(q22q24) syndrome with Potter sequence.
Clark RD
Am J Med Genet; 1984 Dec; 19(4):703-5. PubMed ID: 6517095
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]