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 *

163 related articles for article (PubMed ID: 22965927)

  • 21. Correlates of genetic risk for non-syndromic cleft lip with or without cleft palate.
    Mitchell LE; Risch N
    Clin Genet; 1993 May; 43(5):255-60. PubMed ID: 8375107
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Dominant inheritance of cleft palate, microstomia and micrognathia--possible linkage to the fragile site at 16q22 (FRA16B).
    McKenzie F; Turner A; Withers S; Dalzell P; McGlynn M; Kirk EP
    Clin Dysmorphol; 2002 Oct; 11(4):237-41. PubMed ID: 12401987
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Classification of oral clefts by affection site and laterality: a genotype-phenotype correlation study.
    Farina A; Wyszynski DF; Pezzetti F; Scapoli L; Martinelli M; Carinci F; Carls F; Nardelli GB; Tognon M; Carinci P
    Orthod Craniofac Res; 2002 Aug; 5(3):185-91. PubMed ID: 12194669
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 20p11 deletion in a female child with panhypopituitarism, cleft lip and palate, dysmorphic facial features, global developmental delay and seizure disorder.
    Williams PG; Wetherbee JJ; Rosenfeld JA; Hersh JH
    Am J Med Genet A; 2011 Jan; 155A(1):186-91. PubMed ID: 21204230
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome.
    Santoro C; Riccio S; Palladino F; Aliberti F; Carotenuto M; Zanobio M; Peduto C; Nigro V; Perrotta S; Piluso G
    Eur J Med Genet; 2021 May; 64(5):104190. PubMed ID: 33722742
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):821-826. PubMed ID: 29241927
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Chromosome 22q11 deletion and other chromosome aberrations in cases with cleft palate, congenital heart defects and/or mental disability. A survey based on the Danish Facial Cleft Register.
    Brøndum-Nielsen K; Christensen K
    Clin Genet; 1996 Sep; 50(3):116-20. PubMed ID: 8946108
    [TBL] [Abstract][Full Text] [Related]  

  • 28. MicroRNA-374a, -4680, and -133b suppress cell proliferation through the regulation of genes associated with human cleft palate in cultured human palate cells.
    Suzuki A; Li A; Gajera M; Abdallah N; Zhang M; Zhao Z; Iwata J
    BMC Med Genomics; 2019 Jul; 12(1):93. PubMed ID: 31262291
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A locus for isolated cleft palate, located on human chromosome 2q32.
    Brewer CM; Leek JP; Green AJ; Holloway S; Bonthron DT; Markham AF; FitzPatrick DR
    Am J Hum Genet; 1999 Aug; 65(2):387-96. PubMed ID: 10417281
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Detection and functional analysis of BMP2 gene mutation in patients with tooth agenesis].
    Wang H; Liu Y; Liu HC; Han D; Feng HL
    Beijing Da Xue Xue Bao Yi Xue Ban; 2019 Feb; 51(1):9-15. PubMed ID: 30773537
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome.
    Cafiero C; Marangi G; Orteschi D; Ali M; Asaro A; Ponzi E; Moncada A; Ricciardi S; Murdolo M; Mancano G; Contaldo I; Leuzzi V; Battaglia D; Mercuri E; Slavotinek AM; Zollino M
    Eur J Hum Genet; 2015 Nov; 23(11):1499-504. PubMed ID: 25712080
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The smallest de novo deletion of 20q11.21-q11.23 in a girl with feeding problems, retinal dysplasia, and skeletal abnormalities.
    Posmyk R; Leśniewicz R; Gogiel M; Chorąży M; Bakunowicz-Łazarczyk A; Sielicka D; Vermeesch J; Nowakowska BA
    Am J Med Genet A; 2014 Apr; 164A(4):1056-61. PubMed ID: 24459047
    [TBL] [Abstract][Full Text] [Related]  

  • 33. No justification of routine screening for 22q11 deletions in patients with overt cleft palate.
    Ruiter EM; Bongers EM; Smeets D; Kuijpers-Jagtman AM; Hamel BC
    Clin Genet; 2003 Sep; 64(3):216-9. PubMed ID: 12919136
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Evidence for a microdeletion in 1q32-41 involving the gene responsible for Van der Woude syndrome.
    Sander A; Schmelzle R; Murray J
    Hum Mol Genet; 1994 Apr; 3(4):575-8. PubMed ID: 8069301
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Impact of 22q deletion syndrome on speech outcomes following primary surgery for submucous cleft palate.
    Bezuhly M; Fischbach S; Klaiman P; Fisher DM
    Plast Reconstr Surg; 2012 Mar; 129(3):502e-510e. PubMed ID: 22373999
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Etiological subgroups in non-syndromic isolated cleft palate. A genetic-epidemiological study of 52 Danish birth cohorts.
    Christensen K; Fogh-Andersen P
    Clin Genet; 1994 Nov; 46(5):329-35. PubMed ID: 7889640
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Report of a patient with developmental delay, hearing loss, growth retardation, and cleft lip and palate and a deletion of 7q34-36.1: review of distal 7q deletions.
    Rush ET; Stevens JM; Sanger WG; Olney AH
    Am J Med Genet A; 2013 Jul; 161A(7):1726-32. PubMed ID: 23696251
    [TBL] [Abstract][Full Text] [Related]  

  • 38. De novo 2q36.1q36.3 interstitial deletion involving the PAX3 and EPHA4 genes in a fetus with spina bifida and cleft palate.
    Goumy C; Gay-Bellile M; Eymard-Pierre E; Kemeny S; Gouas L; Déchelotte P; Gallot D; Véronèse L; Tchirkov A; Pebrel-Richard C; Vago P
    Birth Defects Res A Clin Mol Teratol; 2014 Jun; 100(6):507-11. PubMed ID: 24753315
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Array-CGH detection of a de novo 0.8Mb deletion in 19q13.32 associated with mental retardation, cardiac malformation, cleft lip and palate, hearing loss and multiple dysmorphic features.
    Leal T; Andrieux J; Duban-Bedu B; Bouquillon S; Brevière GM; Delobel B
    Eur J Med Genet; 2009; 52(1):62-6. PubMed ID: 19022414
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The 18q deletion syndrome and analysis of the critical region for orofacial cleft at 18q22.3.
    Dostal A; Nemeckova J; Gaillyova R
    J Craniomaxillofac Surg; 2009 Jul; 37(5):272-5. PubMed ID: 19157891
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.