These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
157 related articles for article (PubMed ID: 15937946)
21. Sandrow syndrome of mirror hands and feet and facial abnormalities. Kogekar N; Teebi AS; Vockley J Am J Med Genet; 1993 Apr; 46(2):126-8. PubMed ID: 8387243 [TBL] [Abstract][Full Text] [Related]
22. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome? Rauen KA; Albertson DG; Pinkel D; Cotter PD Am J Med Genet; 2002 Jun; 110(1):51-6. PubMed ID: 12116271 [TBL] [Abstract][Full Text] [Related]
23. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11. Sergi C; Serpi M; Müller-Navia J; Schnabel PA; Hagl S; Otto HF; Ulmer HE Pathologica; 1999 Jun; 91(3):166-72. PubMed ID: 10536461 [TBL] [Abstract][Full Text] [Related]
24. Aplasia cutis congenita, cleft palate, epidermolysis bullosa, and ectrodactyly: a new syndrome? Jones EM; Hersh JH; Yusk JW Pediatr Dermatol; 1992 Sep; 9(3):293-7. PubMed ID: 1488384 [TBL] [Abstract][Full Text] [Related]
25. MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomalies. Witters I; Devriendt K; Spinnewijn D; Moerman P; Van Assche FA; Fryns JP Am J Med Genet; 2002 Jan; 107(3):233-6. PubMed ID: 11807905 [TBL] [Abstract][Full Text] [Related]
26. Further delineation of brain anomalies in velo-cardio-facial syndrome. Altman DH; Altman NR; Mitnick RJ; Shprintzen RJ Am J Med Genet; 1995 Apr; 60(2):174-5. PubMed ID: 7485256 [No Abstract] [Full Text] [Related]
27. Agenesis of tibia with bifid femur, congenital heart disease, and cleft lip with cleft palate or tracheoesophageal fistula: possible variants of Gollop-Wolfgang complex. Erickson RP Am J Med Genet A; 2005 Apr; 134(3):315-7. PubMed ID: 15732065 [TBL] [Abstract][Full Text] [Related]
28. Fryns syndrome with osteochondrodysplasia. Slavotinek AM; Robinson H; Steele MA Am J Med Genet A; 2005 May; 134(4):454-6. PubMed ID: 15793837 [No Abstract] [Full Text] [Related]
30. Case reports of oculofaciocardiodental syndrome with unusual dental findings. Oberoi S; Winder AE; Johnston J; Vargervik K; Slavotinek AM Am J Med Genet A; 2005 Jul; 136(3):275-7. PubMed ID: 15957158 [TBL] [Abstract][Full Text] [Related]
31. Further delineation of the Toriello-Carey syndrome: a report of two siblings. Barisic I; Peter B; Mikecin L Am J Med Genet A; 2003 Jan; 116A(2):188-91. PubMed ID: 12494442 [TBL] [Abstract][Full Text] [Related]
32. Velo-cardio-facial syndrome: a review of 120 patients. Goldberg R; Motzkin B; Marion R; Scambler PJ; Shprintzen RJ Am J Med Genet; 1993 Feb; 45(3):313-9. PubMed ID: 8434617 [TBL] [Abstract][Full Text] [Related]
33. Molecular characterization of a 14q deletion in a boy with features of Holt-Oram syndrome. Le Meur N; Goldenberg A; Michel-Adde C; Drouin-Garraud V; Blaysat G; Marret S; Amara SA; Moirot H; Joly-Hélas G; Mace B; Kleinfinger P; Saugier-Veber P; Frébourg T; Rossi A Am J Med Genet A; 2005 May; 134(4):439-42. PubMed ID: 15810003 [TBL] [Abstract][Full Text] [Related]
34. Spontaneous chylothorax in a case of cardio-facio-cutaneous syndrome. Chan PC; Chiu HC; Hwu WL Clin Dysmorphol; 2002 Oct; 11(4):297-8. PubMed ID: 12401999 [TBL] [Abstract][Full Text] [Related]
35. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review. Leonardi ML; Pai GS; Wilkes B; Lebel RR Am J Med Genet; 2001 Aug; 102(3):237-42. PubMed ID: 11484200 [TBL] [Abstract][Full Text] [Related]
36. CHARGE association-related ocular pathology in a newborn with partial trisomy 19q and partial monosomy 21q, from a maternal translocation (19;21) (q13.1;q22.3). De Krijger RR; Mooy CM; Van Hemel JO; Sulkers EJ; Kros JM; Bartelings MM; Govaerts LC Pediatr Dev Pathol; 1999; 2(6):577-81. PubMed ID: 10508883 [TBL] [Abstract][Full Text] [Related]
37. Fryns syndrome: a new variable multiple congenital anomaly (MCA) syndrome. Lubinsky M; Severn C; Rapoport JM Am J Med Genet; 1983 Mar; 14(3):461-6. PubMed ID: 6859098 [TBL] [Abstract][Full Text] [Related]
38. Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? Grosso S; De Cosmo L; Bonifazi E; Galluzzi P; Farnetani MA; Loffredo P; Anichini C; Berardi R; Morgese G; Balestri P Am J Med Genet A; 2004 Jan; 124A(2):192-5. PubMed ID: 14699619 [TBL] [Abstract][Full Text] [Related]
39. Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome. Descipio C; Schneider L; Young TL; Wasserman N; Yaeger D; Lu F; Wheeler PG; Williams MS; Bason L; Jukofsky L; Menon A; Geschwindt R; Chudley AE; Saraiva J; Schinzel AA; Guichet A; Dobyns WE; Toutain A; Spinner NB; Krantz ID Am J Med Genet A; 2005 Apr; 134A(1):3-11. PubMed ID: 15704124 [TBL] [Abstract][Full Text] [Related]