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Oligohydramnios sequence
Known as:
Potter Syndrome
, Potter's Sequence
, Potter sequence
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A rare, lethal congenital malformation characterized by bilateral renal agenesis and the absence or decreased volume of amniotic fluid…
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National Institutes of Health
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Related topics
Related topics
2 relations
Congenital absence of kidneys syndrome
Hereditary Diseases
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2007
Highly Cited
2007
Total and inorganic arsenic in Antarctic macroalgae.
S. Farías
,
P. Smichowski
,
D. Vélez
,
R. Montoro
,
A. Curtosi
,
C. Vodopívez
Chemosphere
2007
Corpus ID: 6158446
Highly Cited
1997
Highly Cited
1997
MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME 2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, HYPOSPADIAS, AND OLIGOHYDRAMNIOS
WENDY F. Hansen
,
L. Bernard
,
+7 authors
D. Kalousek
Prenatal Diagnosis
1997
Corpus ID: 8837834
We present a case of maternal uniparental heterodisomy for chromosome 2 (UPD 2) detected after trisomy 2 mosaicism was found on…
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Review
1995
Review
1995
Urinary tract anomalies detected by prenatal ultrasound examination at Mayo Clinic Rochester.
J. Gloor
,
P. Ogburn
,
R. Breckle
,
B. Morgenstern
,
D. Milliner
Mayo Clinic proceedings
1995
Corpus ID: 21592072
OBJECTIVE To determine the frequency of fetal urinary tract anomalies and to characterize the types of such abnormalities…
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Review
1993
Review
1993
Fetal Hemivertebrae: Associated Anomalies, Significance, and Outcome
C. Zelop
,
D. Pretorius
Obstetrics and Gynecology
1993
Corpus ID: 32775231
Objective: To study fetuses who had the sonographic diagnosis of hemivertebrae made in utero (excluding open neural tube defects…
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1990
1990
Erythropoietin levels and erythropoiesis at birth in infants with Potter syndrome.
J. Widness
,
A. Philipps
,
G. Clemons
Jornal de Pediatria
1990
Corpus ID: 43262301
1983
1983
Indomethacin and the fetal renal nonfunction syndrome.
D. Veersema
,
P. de Jong
,
J. A. van Wijck
European Journal of Obstetrics, Gynecology, and…
1983
Corpus ID: 32647174
1982
1982
Multiple Acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers
N. Böhm
,
J. Uy
,
M. Kiessling
,
W. Lehnert
European Journal of Pediatrics
1982
Corpus ID: 31551700
The post mortem and microscopic findings of two newborn male sibling of Turkish origin suffering from multiple acyl-CoA…
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1977
1977
Prenatal Diagnosis of Bilateral Renal Agenesis
S. Kaffe
,
L. Godmilow
,
B. Walker
,
K. Hirschhorn
Obstetrics and Gynecology
1977
Corpus ID: 2722021
Bilateral renal agenesis (BRA), or Potter's syndrome, is a rare genetic disorder in which agenesis of the kidneys is associated…
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1974
1974
Unilateral and bilateral renal agenesis in monoamniotic twins.
S. M. Mauer
,
R. S. Dobrin
,
Robert L. Vernier
Jornal de Pediatria
1974
Corpus ID: 30586002
1974
1974
Lung perforation during chest tube placement in the stiff lung syndrome.
A. Wilson
,
H. Krous
Journal of Pediatric Surgery
1974
Corpus ID: 7649941
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