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: 6313864)

  • 1. [Polysyndactyly with complex cardiopathy. Apropos of 3 cases in the same family].
    Bonneau JC; Moirot H; Bastard C; Petitcolas J; Ropartz C
    J Genet Hum; 1983 Jun; 31(2):93-105. PubMed ID: 6313864
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial crossed polysyndactyly.
    Goldstein DJ; Kambouris M; Ward RE
    Am J Med Genet; 1994 Apr; 50(3):215-23. PubMed ID: 8042663
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Autosomal dominant Mendelian midline complex. Secundum atrial septal defect associated with cardiac and facial-thoracic defects. A familial case].
    Stéphan E; Ashoush R; Mégarbané A; Kassab R; Salem N; Loiselet J; Bouvagnet P
    Arch Mal Coeur Vaiss; 2000 May; 93(5):641-7. PubMed ID: 10858865
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hypertelorism, proptosis, ptosis, polysyndactyly, hypospadias and normal height in 3 sibs: a new syndrome?
    Naguib KK
    Am J Med Genet; 1988 Jan; 29(1):35-41. PubMed ID: 2830788
    [No Abstract]   [Full Text] [Related]  

  • 5. Naguib-Richieri-Costa syndrome: hypertelorism, hypospadias, and polysyndactyly syndrome.
    Teebi AS
    Am J Med Genet; 1992 Sep; 44(1):115-7. PubMed ID: 1325738
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. Aplasia cutis congenita, congenital heart lesions, and frontonasal cysts in four successive generations.
    Rodrigues RG
    Clin Genet; 2007 Jun; 71(6):558-60. PubMed ID: 17539905
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A boy with choanal atresia and cardiac defect: Burn-McKeown syndrome?
    Toriello HV; Higgins JV
    Clin Dysmorphol; 1999 Apr; 8(2):143-5. PubMed ID: 10319205
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Melnick-Needles syndrome: indication for an autosomal recessive form.
    ter Haar B; Hamel B; Hendriks J; de Jager J
    Am J Med Genet; 1982 Dec; 13(4):469-77. PubMed ID: 7158646
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Variation in severity of cardiac disease in Holt-Oram syndrome.
    Sletten LJ; Pierpont ME
    Am J Med Genet; 1996 Oct; 65(2):128-32. PubMed ID: 8911604
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Holt-Oram syndrome (apropos of a familial case concerning 5 generations)].
    Giraud F; Bertozzi JB; Mattei JF; Gerard R; Bernard R
    Arch Fr Pediatr; 1974 Oct; 31(8):765-74. PubMed ID: 4462497
    [No Abstract]   [Full Text] [Related]  

  • 12. Holzgreve syndrome: recurrence in sibs.
    Thomas IT; Honore GM; Jewett T; Velvis H; Garber P; Ruiz C
    Am J Med Genet; 1993 Mar; 45(6):767-9. PubMed ID: 8456859
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bonneau syndrome: a further case report.
    Rajab A
    Clin Dysmorphol; 1997 Jan; 6(1):85-8. PubMed ID: 9018424
    [No Abstract]   [Full Text] [Related]  

  • 14. Intrafamilial variability in Fraser syndrome.
    Prasun P; Pradhan M; Goel H
    Prenat Diagn; 2007 Aug; 27(8):778-82. PubMed ID: 17546704
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multiple lentigines syndrome in a Nigerian family.
    Kubeyinje EP; Onunu AN; Obasohan AO
    Trop Geogr Med; 1993; 45(3):135-7. PubMed ID: 8362457
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal death in Fraser syndrome.
    Comstock JM; Putnam AR; Opitz JM; Pysher TJ; Szakacs J
    Fetal Pediatr Pathol; 2005; 24(4-5):223-38. PubMed ID: 16396829
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutchinick syndrome in a Japanese girl.
    Tonoki H; Hattori T; Kamoshida H; Ohta Y; Niikawa N
    Am J Med Genet; 1999 Mar; 83(2):96-9. PubMed ID: 10190479
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).
    Gibbons B; Tan SY; Kee SK; Quaife R; Lim ST
    Am J Med Genet; 1999 Sep; 86(3):289-93. PubMed ID: 10482883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family.
    Arnold GL; Bixler D; Girod D
    Am J Med Genet; 1983 Sep; 16(1):35-42. PubMed ID: 6638068
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Brief clinical report: familial neonatally lethal syndrome of hypoplastic left heart, absent pulmonary lobation, polydactyly, and talipes, probably Smith-Lemli-Opitz (RSH) syndrome.
    Kohler HG
    Am J Med Genet; 1983 Mar; 14(3):423-8. PubMed ID: 6859093
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.