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24. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness. Sommer A; Young-Wee T; Frye T Am J Med Genet; 1983 May; 15(1):71-7. PubMed ID: 6859126 [TBL] [Abstract][Full Text] [Related]
25. A mild form of Roberts/SC phocomelia syndrome with asymmetrical reduction of the upper limbs. Concolino D; Sperlì D; Cinti R; Strisciuglio P; Andria G Clin Genet; 1996 May; 49(5):274-6. PubMed ID: 8832138 [TBL] [Abstract][Full Text] [Related]
26. Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q. Terrett JA; Newbury-Ecob R; Cross GS; Fenton I; Raeburn JA; Young ID; Brook JD Nat Genet; 1994 Apr; 6(4):401-4. PubMed ID: 8054982 [TBL] [Abstract][Full Text] [Related]
27. A radiological and genetic investigation of acheiropody in a kindred including six cases. Toledo SP; Saldanha PH J Genet Hum; 1969 May; 17(1):81-94. PubMed ID: 5808544 [No Abstract] [Full Text] [Related]
28. 'Disorganization-like syndrome' with 47,XXY and unilateral narrowing of the common iliac artery. Woods CG; Treleaven S; Betheras FR; Sheffield LJ Clin Dysmorphol; 1995 Jan; 4(1):82-6. PubMed ID: 7735511 [TBL] [Abstract][Full Text] [Related]
29. The Coffin-Lowry syndrome. Experience from four centres. Hunter AG; Partington MW; Evans JA Clin Genet; 1982 May; 21(5):321-35. PubMed ID: 7116677 [TBL] [Abstract][Full Text] [Related]
30. [Case of leprechaunism in a girl]. Badalian LO; Petrukhin AS; Filina NP Pediatriia; 1980 Dec; (12):24-7. PubMed ID: 7220166 [No Abstract] [Full Text] [Related]
31. Robinow syndrome. Patton MA; Afzal AR J Med Genet; 2002 May; 39(5):305-10. PubMed ID: 12011143 [TBL] [Abstract][Full Text] [Related]
32. Pterygia associated with otomandibular anomalies: a new autosomal recessive condition? Williams DK; McKeever P; Barrow M Clin Dysmorphol; 1997 Apr; 6(2):123-8. PubMed ID: 9134291 [TBL] [Abstract][Full Text] [Related]
33. Concomitant rhomboid-shaped tibiae and fibulae, finger-like projections, and orthopedic management in a new variant of nievergelt syndrome: A case report. Pehlivanoğlu T; Demirel M; Sağlam Y; Balci Hİ; Durmaz H Int J Surg Case Rep; 2018; 42():109-115. PubMed ID: 29245094 [TBL] [Abstract][Full Text] [Related]
34. Symphalangism and brachydactyly syndrome: report of the WL symphalangism-brachydactyly syndrome: review of literature and classification. Herrmann J Birth Defects Orig Artic Ser; 1974; 10(5):23-53. PubMed ID: 4469994 [No Abstract] [Full Text] [Related]
36. A Feingold syndrome case with previously undescribed features and a new mutation. Koçak H; Ozaydin E; Köse G; Marcelis CL; Kamsteeg EJ; Ceylaner S Genet Couns; 2009; 20(3):261-7. PubMed ID: 19852433 [TBL] [Abstract][Full Text] [Related]
37. [The hand-foot-uterus syndrome. A report of a case with recessive autosomal inheritance]. Stella NC; Triolo O; Corrado F Minerva Ginecol; 1993 Sep; 45(9):429-32. PubMed ID: 8255504 [TBL] [Abstract][Full Text] [Related]
38. Four cases of trisomy 18 syndrome with limb reduction malformations. Christianson AL; Nelson MM J Med Genet; 1984 Aug; 21(4):293-7. PubMed ID: 6492096 [TBL] [Abstract][Full Text] [Related]
39. Severe lower limb malformation associated with other deformities and death in infancy in two brothers. Fried K; Goldberg MD; Mundel G; Reif R J Med Genet; 1977 Oct; 14(5):352-4. PubMed ID: 592351 [TBL] [Abstract][Full Text] [Related]