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 *

112 related articles for article (PubMed ID: 11746016)

  • 1. Dominant transmission of a previously unidentified 13/17 translocation in a five-generation family with Robin cleft and other skeletal defects.
    Stalker HJ; Gray BA; Zori RT
    Am J Med Genet; 2001 Nov; 103(4):339-41. PubMed ID: 11746016
    [No Abstract]   [Full Text] [Related]  

  • 2. Variable expression of rib, pectus, and scapular anomalies with Robin-type cleft palate in a 5-generation family: a new syndrome?
    Stalker HJ; Zori RT
    Am J Med Genet; 1997 Dec; 73(3):247-50. PubMed ID: 9415678
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Isolated Robin sequence associated with a balanced t(2;17) chromosomal translocation.
    Jamshidi N; Macciocca I; Dargaville PA; Thomas P; Kilpatrick N; McKinlay Gardner RJ; Farlie PG
    J Med Genet; 2004 Jan; 41(1):e1. PubMed ID: 14729841
    [No Abstract]   [Full Text] [Related]  

  • 4. Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.
    Melkoniemi M; Koillinen H; Männikkö M; Warman ML; Pihlajamaa T; Kääriäinen H; Rautio J; Hukki J; Stofko JA; Cisneros GJ; Krakow D; Cohn DH; Kere J; Ala-Kokko L
    Eur J Hum Genet; 2003 Mar; 11(3):265-70. PubMed ID: 12673280
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Trisomy 3q2 and Pierre-Robin sequence in a boy with unbalanced 46,XY, der(10), t(3;10)(q23;q26.3) de novo karyotype.
    Kleczkowska A; Fryns JP; Moerman F; Martens M; Eggermont E; Jaeken J; Van den Berghe H
    Helv Paediatr Acta; 1988 Nov; 43(3):245-8. PubMed ID: 3220792
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial trisomy 11q in a female infant with Robin sequence and congenital heart disease.
    Wallerstein R; Desposito F; Aviv H; Schenk M; Wallerstein DF
    Cleft Palate Craniofac J; 1992 Jan; 29(1):77-9. PubMed ID: 1547253
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Stickler syndrome. Presenting as a syndrome of cleft palate, myopia and blindness inherited as a dominant trait.
    Hall J
    Birth Defects Orig Artic Ser; 1974; 10(8):157-71. PubMed ID: 4218495
    [No Abstract]   [Full Text] [Related]  

  • 8. Overlap of Patau and Pierre Robin syndromes along with abnormal metabolism: an interesting case study.
    Jaiswal SK; Sukla KK; Gupta V; Rai AK
    J Genet; 2014 Dec; 93(3):865-8. PubMed ID: 25572249
    [No Abstract]   [Full Text] [Related]  

  • 9. [Genetic studies in Pierre Robin syndrome].
    Jörgensen G; Freund HJ
    ZWR; 1979 Nov; 88(21):958-60. PubMed ID: 294009
    [No Abstract]   [Full Text] [Related]  

  • 10. Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12). Letter.
    Balci S; Aypar E; Engiz O
    Cleft Palate Craniofac J; 2010 Jul; 47(4):431-2. PubMed ID: 20163253
    [No Abstract]   [Full Text] [Related]  

  • 11. Altered mandibular development precedes the time of palate closure in mice homozygous for disproportionate micromelia: an oral clefting model supporting the Pierre-Robin sequence.
    Ricks JE; Ryder VM; Bridgewater LC; Schaalje B; Seegmiller RE
    Teratology; 2002 Mar; 65(3):116-20. PubMed ID: 11877774
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cleft lip and/or palate: 10 years experience at a pediatric cleft center in Southern Thailand.
    Jaruratanasirikul S; Chichareon V; Pattanapreechawong N; Sangsupavanich P
    Cleft Palate Craniofac J; 2008 Nov; 45(6):597-602. PubMed ID: 18956943
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The genetic basis of the Pierre Robin Sequence.
    Jakobsen LP; Knudsen MA; Lespinasse J; García Ayuso C; Ramos C; Fryns JP; Bugge M; Tommerup N
    Cleft Palate Craniofac J; 2006 Mar; 43(2):155-9. PubMed ID: 16526920
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dominant transmission of Sprengel's shoulder and cleft palate.
    Hodgson SV; Chiu DC
    J Med Genet; 1981 Aug; 18(4):263-5. PubMed ID: 7277418
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stickler syndrome in a pedigree of Pierre Robin syndrome.
    Schreiner RL; McAlister WH; Marshall RE; Shearer WT
    Am J Dis Child; 1973 Jul; 126(1):86-90. PubMed ID: 4198747
    [No Abstract]   [Full Text] [Related]  

  • 16. Association of autosomal dominant cleft lip and palate and translocation 6p23;9q22.3.
    Donnai D; Heather LJ; Sinclair P; Thakker Y; Scambler PJ; Dixon MJ
    Clin Dysmorphol; 1992 Apr; 1(2):89-97. PubMed ID: 1345518
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pierre Robin syndrome occurring in two related sibships.
    Bixler D; Christian JC
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):67-71. PubMed ID: 5173245
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Translocation (13;17)(q14;q25) as a novel chromosomal abnormality in acute myeloid leukemia-M4.
    Turhan N; Yürür-Kutlay N; Topcuoglu P; Sayki M; Yüksel M; Gürman G; Tükün A
    Leuk Res; 2006 Jul; 30(7):903-5. PubMed ID: 16469377
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Abnormal facies, cleft palate, and generalized dysostosis: a lethal X-linked syndrome.
    André M; Vigneron J; Didier F
    J Pediatr; 1981 May; 98(5):747-52. PubMed ID: 7229752
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Association of male XX with Pierre Robin syndrome in a child whose father has a balanced 46XY, t (16; 17) (p13;q21) translocation].
    Petrus M; Bourrouillou G; Dutau G; Colombies P; Rochiccioli P
    J Genet Hum; 1981 Jun; 29(2):191-6. PubMed ID: 7199077
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.