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2. [Cryptophthalmia and associated malformations in a consanguine African milieu (South Mauritania)]. Chovet M; Dufour J; Degabriel J Med Trop (Mars); 1972; 32():Suppl:419-26. PubMed ID: 4629845 [No Abstract] [Full Text] [Related]
4. [Fryns syndrome: report of the first case in the national literature]. Rentería-Ibarra M; Frías-Márquez SG; Michel-Aceves RJ; Navarrete-Arellano M Bol Med Hosp Infant Mex; 1993 Sep; 50(9):666-70. PubMed ID: 8373549 [TBL] [Abstract][Full Text] [Related]
5. A sibship with unusual anomalies of the eye and skeleton (Michels' syndrome). De La Paz MA; Lewis RA; Patrinely JR; Merin L; Greenberg F Am J Ophthalmol; 1991 Nov; 112(5):572-80. PubMed ID: 1951596 [TBL] [Abstract][Full Text] [Related]
6. Ocular abnormalities in craniofacial malformations. Miller MT Int Ophthalmol Clin; 1984; 24(1):143-63. PubMed ID: 6443567 [No Abstract] [Full Text] [Related]
8. [Congenital blepharophimosis, ptosis and epicanthus inversus in a Balinese (Indonesia) family]. Ney R; Breguet G Rev Med Suisse Romande; 1981 Apr; 101(4):269-72. PubMed ID: 7256058 [No Abstract] [Full Text] [Related]
9. Bone and joint manifestations of Rieger's syndrome: a report of a family. Koshino T; Konno T; Ohzeki T J Pediatr Orthop; 1989; 9(2):224-30. PubMed ID: 2494224 [TBL] [Abstract][Full Text] [Related]
10. Syndrome identification case report 90: multiple craniofacial and skeletal defects. Mastroiacovo P; De Rosa G; Satta MA; Colavita N; Priolo F; Pasargiklian E J Clin Dysmorphol; 1983; 1(1):13-5. PubMed ID: 6580383 [No Abstract] [Full Text] [Related]
11. Hypospadias as a new congenital anomaly in Bowen-Conradi syndrome. Aynaci FM; Mocan H; Erduran E; Gedik Y Genet Couns; 1994; 5(4):369-71. PubMed ID: 7888139 [No Abstract] [Full Text] [Related]
12. The radiology of Coffin-Lowry syndrome. Padley S; Hodgson SV; Sherwood T Br J Radiol; 1990 Jan; 63(745):72-5. PubMed ID: 2306591 [No Abstract] [Full Text] [Related]
13. Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: a new syndrome? Chitayat D; Haj-Chahine S; Stalker HJ; Azouz EM; Côté A; Halal F Am J Med Genet; 1993 Jan; 45(1):1-4. PubMed ID: 8418638 [TBL] [Abstract][Full Text] [Related]
14. Craniomyeloschisis: a spontaneous mutation of the rat. Layton WM; Smith JM Teratology; 1977 Apr; 15(2):171-7. PubMed ID: 867275 [TBL] [Abstract][Full Text] [Related]
17. Apparent Greig cephalopolysyndactyly and sinus node disease. Fryns JP; De Waele P; Van der Hauwaert L; Van den Berghe H Am J Med Genet; 1993 Jan; 45(1):38-40. PubMed ID: 8418656 [TBL] [Abstract][Full Text] [Related]
18. Generalized osseous abnormalities in the Marshall syndrome. O'Donnell JJ; Sirkin S; Hall BD Birth Defects Orig Artic Ser; 1976; 12(5):299-314. PubMed ID: 953235 [No Abstract] [Full Text] [Related]
19. Mosaic trisomy 9 syndrome with unusual phenotype. Kaminker CP; Daín L; Lamas MA; Sánchez JM Am J Med Genet; 1985 Oct; 22(2):237-41. PubMed ID: 3931476 [TBL] [Abstract][Full Text] [Related]
20. Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly. Münke M Am J Med Genet; 1989 Oct; 34(2):237-45. PubMed ID: 2683787 [No Abstract] [Full Text] [Related] [Next] [New Search]