-
1
-
-
0043143186
-
Pathogenesis of polycystic kidneys. Historical survey
-
Osathanondh V., Potter E.L. Pathogenesis of polycystic kidneys. Historical survey. Arch Pathol. 77:1964;459-465.
-
(1964)
Arch Pathol
, vol.77
, pp. 459-465
-
-
Osathanondh, V.1
Potter, E.L.2
-
2
-
-
0013636188
-
Zystische Nierenerkrankungen-Klassifikation und neue Aspekte
-
Zerres K., Waldherr R. Zystische Nierenerkrankungen-Klassifikation und neue Aspekte. Dt Ärzteblatt. 87:(43):1990;2356-2362.
-
(1990)
Dt Ärzteblatt
, vol.87
, Issue.43
, pp. 2356-2362
-
-
Zerres, K.1
Waldherr, R.2
-
4
-
-
0023572309
-
Genetics of cystic kidney diseases
-
Zerres K. Genetics of cystic kidney diseases. Pediatr Nephrol. 1:1987;397-404.
-
(1987)
Pediatr Nephrol
, vol.1
, pp. 397-404
-
-
Zerres, K.1
-
5
-
-
0013656486
-
Molekulare Genetik von Nierenerkrankungen
-
Hildebrandt F., Weber M., Brandis M. Molekulare Genetik von Nierenerkrankungen. Dt Ärzteblatt. 93:(7):1996;308-313.
-
(1996)
Dt Ärzteblatt
, vol.93
, Issue.7
, pp. 308-313
-
-
Hildebrandt, F.1
Weber, M.2
Brandis, M.3
-
6
-
-
0028708768
-
Zystische Nierendysplasie variabler Ausprägung-Pränatalsonografische, zytogenetische und patho-anatomische Befunde anhand von drei Fallbeispielen
-
Tennstedt C., Bollman R., Chaoui R., Cobet G., Körner H., Kirchmair F. Zystische Nierendysplasie variabler Ausprägung-Pränatalsonografische, zytogenetische und patho-anatomische Befunde anhand von drei Fallbeispielen. Zentralbl Gynäkol. 116:1994;649-654.
-
(1994)
Zentralbl Gynäkol
, vol.116
, pp. 649-654
-
-
Tennstedt, C.1
Bollman, R.2
Chaoui, R.3
Cobet, G.4
Körner, H.5
Kirchmair, F.6
-
7
-
-
0028891499
-
Management of prenatally detected fetal hydronephrosis
-
Gloor J.M. Management of prenatally detected fetal hydronephrosis. Mayo Clin Proc. 70:(2):1995;145-152.
-
(1995)
Mayo Clin Proc
, vol.70
, Issue.2
, pp. 145-152
-
-
Gloor, J.M.1
-
8
-
-
0013658765
-
Genitourinary malformations
-
D.K. James, P.J. Steer, C.P. Weiner, & B. Gonik. WB Saunders Comp LH
-
Holzgreve W., Miny P, Evans M.I. Genitourinary malformations. James D.K., Steer P.J., Weiner C.P., Gonik B., High Risk Pregnancy. 1994;901-916 WB Saunders Comp LH.
-
(1994)
High Risk Pregnancy
, pp. 901-916
-
-
Holzgreve, W.1
Miny P2
Evans, M.I.3
-
9
-
-
0028980029
-
The locus for Meckel syndrome with multiple congenital maps to chromosome 17q21-q24
-
Paavola P., Salonen R., Weissenbach J., Peltonen L. The locus for Meckel syndrome with multiple congenital maps to chromosome 17q21-q24. Nat Genet. 11:(2):1995;213-215.
-
(1995)
Nat Genet
, vol.11
, Issue.2
, pp. 213-215
-
-
Paavola, P.1
Salonen, R.2
Weissenbach, J.3
Peltonen, L.4
-
10
-
-
0029901863
-
Meckel Gruber syndrome
-
Flesso A., Rempen A., Schmausser B., Marx A. Meckel Gruber syndrome. Z Geburtsh Neonatol. 200:(2):1996;66-68.
-
(1996)
Z Geburtsh Neonatol
, vol.200
, Issue.2
, pp. 66-68
-
-
Flesso, A.1
Rempen, A.2
Schmausser, B.3
Marx, A.4
-
12
-
-
0026871729
-
Cardiac rhabdomyoma in tuberous sclerosis. A report of five cases and review of the literature
-
Bosio M., Vitali G.M., Pandolfi M., Pastori P. Cardiac rhabdomyoma in tuberous sclerosis. A report of five cases and review of the literature. Minerva Pediatr. 44:1992;305-311.
-
(1992)
Minerva Pediatr
, vol.44
, pp. 305-311
-
-
Bosio, M.1
Vitali, G.M.2
Pandolfi, M.3
Pastori, P.4
-
13
-
-
19144371868
-
A genetic register for von Hippel-Lindau disease
-
Maddoch I.R., Moran A., Maher E.R., Tease M.D., Norman A., Payne S.J., Whitehouse R., Dodd C., Lavin M., Hartley N., Supos M., Evans D.G. A genetic register for von Hippel-Lindau disease. J Med Genet. 33:(2):1996;120-127.
-
(1996)
J Med Genet
, vol.33
, Issue.2
, pp. 120-127
-
-
Maddoch, I.R.1
Moran, A.2
Maher, E.R.3
Tease, M.D.4
Norman, A.5
Payne, S.J.6
Whitehouse, R.7
Dodd, C.8
Lavin, M.9
Hartley, N.10
Supos, M.11
Evans, D.G.12
-
14
-
-
0025816317
-
Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis
-
Maher E.R., Bentley E., Yates J.R., Latif F., Lerman M., Zbar B., Affara N.A., Ferguson-Smith M. Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis. Genomics. 10:(4):1991;957-960.
-
(1991)
Genomics
, vol.10
, Issue.4
, pp. 957-960
-
-
Maher, E.R.1
Bentley, E.2
Yates, J.R.3
Latif, F.4
Lerman, M.5
Zbar, B.6
Affara, N.A.7
Ferguson-Smith, M.8
-
15
-
-
0029648832
-
Branchio-oto-renal syndrome. 4 cases in three families
-
Basse F., Lacombe D., Abousleiman J., Pauly P., De Martin A. Branchio-oto-renal syndrome. 4 cases in three families. Presse-Med. 24:(18):1995;842-844.
-
(1995)
Presse-Med
, vol.24
, Issue.18
, pp. 842-844
-
-
Basse, F.1
Lacombe, D.2
Abousleiman, J.3
Pauly, P.4
De Martin, A.5
-
16
-
-
0019165942
-
Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss
-
Fraser F.C., Sproule J.R., Halal F. Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss. Am J Med Genet. 7:1980;341-349.
-
(1980)
Am J Med Genet
, vol.7
, pp. 341-349
-
-
Fraser, F.C.1
Sproule, J.R.2
Halal, F.3
-
17
-
-
0020585220
-
Prenatal diagnosis of a short rib-polydactyly syndrome type Salidino-Noonan at 17 weeks gestation
-
Grote W., Weisner D., Jänig U., Harms D., Weidemann H.R. Prenatal diagnosis of a short rib-polydactyly syndrome type Salidino-Noonan at 17 weeks gestation. Eur J Pediatr. 140:1983;63-66.
-
(1983)
Eur J Pediatr
, vol.140
, pp. 63-66
-
-
Grote, W.1
Weisner, D.2
Jänig, U.3
Harms, D.4
Weidemann, H.R.5
-
18
-
-
0027442137
-
Lung hypoplasia, renal failure, and direct hyperbilirubinemia in a newborn infant
-
Harms K., Klinge O., Speer C.P. Lung hypoplasia, renal failure, and direct hyperbilirubinemia in a newborn infant. Monatsschr Kinderheilk. 141:(11):1993;868-873.
-
(1993)
Monatsschr Kinderheilk
, vol.141
, Issue.11
, pp. 868-873
-
-
Harms, K.1
Klinge, O.2
Speer, C.P.3
-
20
-
-
0021253067
-
Oro-facio-digital syndromes I and II: Radiological methods for diagnosis and the clinical variation
-
Anneren G., Arvidson B., Gustovson K.H., Jorulf H., Carlsson G. Oro-facio-digital syndromes I and II: radiological methods for diagnosis and the clinical variation. Clin Genet. 26:1984;178-186.
-
(1984)
Clin Genet
, vol.26
, pp. 178-186
-
-
Anneren, G.1
Arvidson, B.2
Gustovson, K.H.3
Jorulf, H.4
Carlsson, G.5
-
21
-
-
0024319361
-
Prenatal diagnosis and prevention of inherited abnormalities of collagen
-
Pope F.M., Daw S.C.M., Narcisi P. Prenatal diagnosis and prevention of inherited abnormalities of collagen. J Inherit Metab Dis. 12:1989;135-173.
-
(1989)
J Inherit Metab Dis
, vol.12
, pp. 135-173
-
-
Pope, F.M.1
Daw, S.C.M.2
Narcisi, P.3
-
23
-
-
0023821757
-
Prune belly syndrome: Prenatal diagnosis and obstetric procedure
-
Gnirs S., Boos R., Waldherr R., Schmidt W. Prune belly syndrome: prenatal diagnosis and obstetric procedure. Z Geburtshilfe Perinatol. 192:(3):1988;114-121.
-
(1988)
Z Geburtshilfe Perinatol
, vol.192
, Issue.3
, pp. 114-121
-
-
Gnirs, S.1
Boos, R.2
Waldherr, R.3
Schmidt, W.4
-
24
-
-
0020567547
-
Chromosome anomalies in infants with prune belly anomaly: Association with trisomy
-
Frydman M., Magenis R.E., Mohandas T.K., Kaback M.M. Chromosome anomalies in infants with prune belly anomaly: association with trisomy. Am J Med Genet. 15:1983;145-148.
-
(1983)
Am J Med Genet
, vol.15
, pp. 145-148
-
-
Frydman, M.1
Magenis, R.E.2
Mohandas, T.K.3
Kaback, M.M.4
-
25
-
-
0028878839
-
A descriptive study of prune belly in New York State, 1983 to 1989
-
Druschel C.M. A descriptive study of prune belly in New York State, 1983 to 1989. Arch Pediatr Adolesc Med. 149:(1):1995;70-76.
-
(1995)
Arch Pediatr Adolesc Med
, vol.149
, Issue.1
, pp. 70-76
-
-
Druschel, C.M.1
-
26
-
-
0018402867
-
Urethral obstruction malformation complex: A cause of abdominal muscle deficiency and the "prune belly"
-
Pagon R., Smith D., Shepart T. Urethral obstruction malformation complex: a cause of abdominal muscle deficiency and the "prune belly" J Pediatr. 94:1976;900-906.
-
(1976)
J Pediatr
, vol.94
, pp. 900-906
-
-
Pagon, R.1
Smith, D.2
Shepart, T.3
-
27
-
-
0022569811
-
Vater association and anorectal malformations
-
Rintala R., Lindahl H., Louhimo I. Vater association and anorectal malformations. Z Kinderchir. 41:(1):1986;22-26.
-
(1986)
Z Kinderchir
, vol.41
, Issue.1
, pp. 22-26
-
-
Rintala, R.1
Lindahl, H.2
Louhimo, I.3
-
28
-
-
0026692188
-
Morbidity and mortality in 46 patients with the VACTERL association
-
Iuchtmann M., Brereton R., Spitz L., Kiely E.M., Drake D. Morbidity and mortality in 46 patients with the VACTERL association. Isr J Med Sci. 28:(5):1992;281-284.
-
(1992)
Isr J Med Sci
, vol.28
, Issue.5
, pp. 281-284
-
-
Iuchtmann, M.1
Brereton, R.2
Spitz, L.3
Kiely, E.M.4
Drake, D.5
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