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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

114 related articles for article (PubMed ID: 3585941)

  • 21. Fryns syndrome: a predictable, lethal pattern of multiple congenital anomalies.
    Samueloff A; Navot D; Birkenfeld A; Schenker JG
    Am J Obstet Gynecol; 1987 Jan; 156(1):86-8. PubMed ID: 3799773
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Two fetuses with Fryns syndrome without diaphragmatic defects.
    Wilgenbus KK; Engers R; Crombach G; Majewski F
    J Med Genet; 1994 Dec; 31(12):962-4. PubMed ID: 7891381
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.
    Cunniff C; Jones KL; Saal HM; Stern HJ
    Pediatrics; 1990 Apr; 85(4):499-504. PubMed ID: 2314962
    [TBL] [Abstract][Full Text] [Related]  

  • 24. RAPADILINO syndrome.
    Vargas FR; de Almeida JC; Llerena Júnior JC; Reis DF
    Am J Med Genet; 1992 Dec; 44(6):716-9. PubMed ID: 1481838
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Limb/pelvis-hypoplasia/aplasia syndrome--further delineation of phenotype.
    Gupta N; Kabra M
    Fetal Pediatr Pathol; 2011; 30(6):355-8. PubMed ID: 21895521
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fryns syndrome survivors and neurologic outcome.
    Van Hove JL; Spiridigliozzi GA; Heinz R; McConkie-Rosell A; Iafolla AK; Kahler SG
    Am J Med Genet; 1995 Nov; 59(3):334-40. PubMed ID: 8599357
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pallister-Killian and Fryns syndromes.
    Stratton RF; Moore CM; Popham CS; DuPont BR; Mattern VL
    Am J Med Genet; 1994 May; 51(1):90. PubMed ID: 8030681
    [No Abstract]   [Full Text] [Related]  

  • 28. [Prenatal diagnosis of a case of Fryns' syndrome].
    Barthe B; Cohen H; Saada P
    J Gynecol Obstet Biol Reprod (Paris); 1995; 24(1):57-62. PubMed ID: 7730569
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Robinow syndrome. Description of a case with diaphragmatic relaxation].
    Calandi C; Giovannucci ML; Strano M; Pieroni P; Adami-Lami C
    Pediatr Med Chir; 1986; 8(3):429-32. PubMed ID: 3786208
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Atypical Fryns syndrome: clinical, radiological and pathological findings.
    Aygün MS; Sekmenli T; Çiftçi İ; Gökmen Z; Tolu İ; Mutlu-Aygün F
    Turk J Pediatr; 2014; 56(1):107-10. PubMed ID: 24827959
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Specific acromesomelia with facial and renal anomalies: a new syndrome.
    Pfeiffer RA; Hirschfelder H; Rott HD
    Clin Dysmorphol; 1995 Jan; 4(1):38-43. PubMed ID: 7735504
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Fryns syndrome. Report on 3 new cases].
    Alessandri JL; Attali T; Brayer C; Dupuy L; Pilorget H; Ramful D; Samperiz S; Tiran-Rajaofera I; Robin S
    Arch Pediatr; 2007 Jul; 14(7):903-7. PubMed ID: 17442547
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Diaphragmatic defects, limb deficiencies, and ossification defects of the skull: a distinctive malformation syndrome.
    Froster UG; Kolditz P; Wisser J; Robbiani MB; Stallmach T; Hebisch G; Huch R; Huch A
    Am J Med Genet; 1996 Mar; 62(1):48-53. PubMed ID: 8779324
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Congenital anomalies in Duane's retraction syndrome.
    Pfaffenbach DD; Cross HE; Kearns TP
    Arch Ophthalmol; 1972 Dec; 88(6):635-9. PubMed ID: 4628563
    [No Abstract]   [Full Text] [Related]  

  • 35. Amniotic band sequence: Streeter hypothesis revisited.
    Bamforth JS
    Birth Defects Orig Artic Ser; 1993; 29(1):279-89. PubMed ID: 8280880
    [No Abstract]   [Full Text] [Related]  

  • 36. Infant with midline thoracoabdominal schisis and limb defects.
    Pivnick EK; Kaufman RA; Velagaleti GV; Gunther WM; Abramovici D
    Teratology; 1998 Nov; 58(5):205-8. PubMed ID: 9839359
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Split hand/split foot, syndactyly, urinary tract obstruction, radial, diaphragmatic, and neural tube defects: Czeizel-Losonci syndrome?
    Genuardi M; Silvestri E; Tozzi C
    Am J Med Genet; 1994 Jul; 51(3):247-50. PubMed ID: 8074153
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Eye abnormalities in Fryns syndrome.
    Pierson DM; Taboada E; Butler MG
    Am J Med Genet A; 2004 Mar; 125A(3):273-7. PubMed ID: 14994236
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Bartsocas-Papas syndrome with internal anomalies: evidence for a more generalized epithelial defect or new syndrome?
    Hennekam RC; Huber J; Variend D
    Am J Med Genet; 1994 Nov; 53(2):102-7. PubMed ID: 7856636
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Fryns syndrome: a lethal birth defect with variable phenotypic expressions in siblings.
    Arora K; Thukral A; Das RR; Gupta N; Kabra M; Agarwal R
    Indian J Pediatr; 2014 Jun; 81(6):614-6. PubMed ID: 23604607
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.