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2. [Positive diagnosis of Potter's syndrome by ultrasonography. A case report]. Garba H; Dechivré J; Broussard P Rev Fr Gynecol Obstet; 1993 Mar; 88(3):156-61. PubMed ID: 8493446 [TBL] [Abstract][Full Text] [Related]
3. The pathogenesis of Potter's syndrome of renal agenesis. Fitch N; Lachance RC Can Med Assoc J; 1972 Oct; 107(7):653-6. PubMed ID: 4665096 [TBL] [Abstract][Full Text] [Related]
4. Discordance for Potter's Syndrome in a Dichorionic Diamniotic Twin Pregnancy-An Unusual Case Report. Kostov S; Slavchev S; Dzhenkov D; Strashilov S; Yordanov A Medicina (Kaunas); 2020 Mar; 56(3):. PubMed ID: 32143317 [TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of pseudothalidomide syndrome in consecutive pregnancies of a consanguineous couple. Petrikovsky BM; Gross B; Bialer M; Solamanzadeh K; Simhaee E Ultrasound Obstet Gynecol; 1997 Dec; 10(6):425-8. PubMed ID: 9476331 [TBL] [Abstract][Full Text] [Related]
6. Early diagnosis of triploidy. Ranzini AC; Sharma S; Soriano C; Vintzileos AM Ultrasound Obstet Gynecol; 1997 Dec; 10(6):443-4. PubMed ID: 9476333 [No Abstract] [Full Text] [Related]
7. Diagnosis of fetal abnormalities at the 10-14-week scan. Souka AP; Nicolaides KH Ultrasound Obstet Gynecol; 1997 Dec; 10(6):429-42. PubMed ID: 9476332 [No Abstract] [Full Text] [Related]
8. [Fetal plexus cysts. An indication for prenatal karyotyping]. Werner-von der Burg W; Hatzmann W; Kuchenbecker K Geburtshilfe Frauenheilkd; 1992 Nov; 52(11):674-80. PubMed ID: 1452002 [TBL] [Abstract][Full Text] [Related]
9. Potter's syndrome and chromosomal anomalies. Côté GB Hum Genet; 1981; 58(2):220. PubMed ID: 7287008 [No Abstract] [Full Text] [Related]
10. [Potter's syndrome and polycystic kidney in the newborn]. Pasquier B; Couderc P; Bost M; Rambaud P Sem Hop; 1971 Dec; 47(49):2779-88. PubMed ID: 4335740 [No Abstract] [Full Text] [Related]
11. [Potter's syndrome with caudal appendix and feminine pseudohermaphroditism]. Walbaum R; Dehaène P; Houcke M Pediatrie; 1971 Sep; 26(6):649-54. PubMed ID: 5116345 [No Abstract] [Full Text] [Related]
13. LADD syndrome in five members of a three-generation family and prenatal diagnosis. Francannet C; Vanlieferinghen P; Dechelotte P; Urbain MF; Campagne D; Malpuech G Genet Couns; 1994; 5(1):85-91. PubMed ID: 8031542 [TBL] [Abstract][Full Text] [Related]
15. [Renal tubular dysgenesis with fetal renal vein thrombosis]. Ortmann M; Querfeld U; Stollorz M; Schröder R Pathologe; 1995 Mar; 16(2):143-7. PubMed ID: 7761360 [TBL] [Abstract][Full Text] [Related]
16. On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene. Alembik Y; Stoll C; Messer J Genet Couns; 1997; 8(2):133-7. PubMed ID: 9219012 [TBL] [Abstract][Full Text] [Related]
17. FHR patterns in Potter's Syndrome. Peleg D; Dicker D; Samuel N; Feldberg D; Goldman JA J Perinat Med; 1983; 11(3):179-82. PubMed ID: 6875791 [TBL] [Abstract][Full Text] [Related]