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8. Congenital cystic adenomatoid malformation in bilateral renal agenesis. Its mitigation of Potter's syndrome. Krous HF; Harper PE; Perlman M Arch Pathol Lab Med; 1980 Jul; 104(7):368-70. PubMed ID: 6893124 [TBL] [Abstract][Full Text] [Related]
9. Skeletal manifestations in Fryns syndrome. Tsukahara M; Sase M; Tateishi H; Saito T; Kato H; Furukawa S Am J Med Genet; 1995 Jan; 55(2):217-20. PubMed ID: 7717421 [TBL] [Abstract][Full Text] [Related]
10. New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement. Borochowitz Z; Pavone L; Mazor G; Rizzo R; Dar H Am J Med Genet; 1992 Jul; 43(4):678-85. PubMed ID: 1621757 [TBL] [Abstract][Full Text] [Related]
11. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome. Schrander-Stumpel C; de Die-Smulders C; Fryns JP; da Costa J; Bouckaert P Am J Med Genet; 1990 Sep; 37(1):133-5. PubMed ID: 2240030 [TBL] [Abstract][Full Text] [Related]
14. Cerebro-oculo-facio-skeletal syndrome. Insler MS Ann Ophthalmol; 1987 Feb; 19(2):54-5. PubMed ID: 3551738 [TBL] [Abstract][Full Text] [Related]
15. Cerebro-oculo-facio-skeletal syndrome: further delineation. Gershoni-Baruch R; Ludatscher RM; Lichtig C; Sujov P; Machoul I Am J Med Genet; 1991 Oct; 41(1):74-7. PubMed ID: 1951466 [TBL] [Abstract][Full Text] [Related]
16. Cerebro-oculo-facio-skeletal syndrome: report of two cases from Turkey with postmortem findings. Semerci CN; Onat N; Günçe S; Demirel N; Yilmazer MB; Oznur I; Türkyilmaz C; Balci S Turk J Pediatr; 2002; 44(3):269-73. PubMed ID: 12405446 [TBL] [Abstract][Full Text] [Related]
17. Café au lait macules and cerebro-oculo-facio-skeletal syndrome: a novel association. Twede JV; Difazio M Pediatr Dermatol; 2009; 26(1):97-9. PubMed ID: 19250421 [TBL] [Abstract][Full Text] [Related]
18. Congenital cataract, microphthalmia, hypoplasia of corpus callosum and hypogenitalism: report and review of Micro syndrome. Derbent M; Agras PI; Gedik S; Oto S; Alehan F; Saatçi U Am J Med Genet A; 2004 Jul; 128A(3):232-4. PubMed ID: 15216542 [TBL] [Abstract][Full Text] [Related]
19. Severe case of Al Awadi/Raas-Rothschild syndrome or new, possibly autosomal recessive facio-skeleto-genital syndrome. Mollica F; Mazzone D; Cimino G; Opitz JM Am J Med Genet; 1995 Mar; 56(2):168-72. PubMed ID: 7625440 [TBL] [Abstract][Full Text] [Related]
20. [Bilateral renal agenesis or Potter's sequence. A case of recurrent bilateral renal agenesis]. Néophytou O J Gynecol Obstet Biol Reprod (Paris); 1994; 23(1):75-7. PubMed ID: 8157895 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]