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 *

125 related articles for article (PubMed ID: 19996736)

  • 1. A new case of MOMO syndrome.
    Wallerstein R; Sugalski RD
    Clin Dysmorphol; 2010 Jan; 19(1):1-4. PubMed ID: 19996736
    [TBL] [Abstract][Full Text] [Related]  

  • 2. MOMO syndrome: a possible third case.
    Zannolli R; Mostardini R; Hadjistilianou T; Rosi A; Berardi R; Morgese G
    Clin Dysmorphol; 2000 Oct; 9(4):281-4. PubMed ID: 11045586
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Macrocephaly, obesity, mental (intellectual) disability, and ocular abnormalities: alternative definition and further delineation of MOMO syndrome.
    Di Donato N; Riess A; Hackmann K; Rump A; Huebner A; von der Hagen M; Hahn G; Schrock E; Tinschert S
    Am J Med Genet A; 2012 Nov; 158A(11):2857-62. PubMed ID: 22821547
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Coloboma and other ophthalmologic anomalies in Kabuki syndrome: distinction from charge association.
    Ming JE; Russell KL; Bason L; McDonald-McGinn DM; Zackai EH
    Am J Med Genet A; 2003 Dec; 123A(3):249-52. PubMed ID: 14608645
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Kabuki syndrome is not caused by an 8p duplication: a cytogenetic study in 20 patients.
    Engelen JJ; Loneus WH; Vaes-Peeters G; Schrander-Stumpel CT
    Am J Med Genet A; 2005 Jan; 132A(3):276-7. PubMed ID: 15578614
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Macrosomia, obesity, macrocephaly and ocular abnormalities (MOMO syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndrome.
    Moretti-Ferreira D; Koiffmann CP; Listik M; Setian N; Wajntal A
    Am J Med Genet; 1993 Jun; 46(5):555-8. PubMed ID: 8322820
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A homozygous balanced reciprocal translocation suggests LINC00237 as a candidate gene for MOMO (macrosomia, obesity, macrocephaly, and ocular abnormalities) syndrome.
    Vu PY; Toutain J; Cappellen D; Delrue MA; Daoud H; El Moneim AA; Barat P; Montaubin O; Bonnet F; Dai ZQ; Philippe C; Tran CT; Rooryck C; Arveiler B; Saura R; Briault S; Lacombe D; Taine L
    Am J Med Genet A; 2012 Nov; 158A(11):2849-56. PubMed ID: 23034868
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Patellar dislocation in Kabuki syndrome.
    Kurosawa K; Kawame H; Ochiai Y; Nakashima M; Tohma T; Ohashi H
    Am J Med Genet; 2002 Mar; 108(2):160-3. PubMed ID: 11857567
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Symptomatic Chiari I malformation in Kabuki syndrome.
    Ciprero KL; Clayton-Smith J; Donnai D; Zimmerman RA; Zackai EH; Ming JE
    Am J Med Genet A; 2005 Jan; 132A(3):273-5. PubMed ID: 15523623
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Psychological and cognitive evaluation of autism in a patient with MOMO syndrome: a case report and literature review.
    Passalacqua C; García M; Sepúlveda E; Toledo D; Valencia M; Arancibia M
    Medwave; 2019 May; 19(4):e7622. PubMed ID: 31075093
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Further delineation of Kabuki syndrome in 48 well-defined new individuals.
    Armstrong L; Abd El Moneim A; Aleck K; Aughton DJ; Baumann C; Braddock SR; Gillessen-Kaesbach G; Graham JM; Grebe TA; Gripp KW; Hall BD; Hennekam R; Hunter A; Keppler-Noreuil K; Lacombe D; Lin AE; Ming JE; Kokitsu-Nakata NM; Nikkel SM; Philip N; Raas-Rothschild A; Sommer A; Verloes A; Walter C; Wieczorek D; Williams MS; Zackai E; Allanson JE
    Am J Med Genet A; 2005 Jan; 132A(3):265-72. PubMed ID: 15690370
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Macrostomia, thin upper vermilion border, long philtrum, broad halluces, and intellectual disability in two sibs.
    Nampoothiri S; Kuthiroly S; Fauth C; Krabichler B; Attie-Bitach T; Hennekam RC
    Am J Med Genet A; 2011 Oct; 155A(10):2465-8. PubMed ID: 21910233
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sibs with developmental delay, hirsutism and nail hypoplasia: a new syndrome.
    Stewart H; Kerr B; Tomlin P; Stacey D; Super M
    Clin Dysmorphol; 2000 Oct; 9(4):241-6. PubMed ID: 11045578
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Developmental outcome in Kabuki syndrome.
    Vaux KK; Jones KL; Jones MC; Schelley S; Hudgins L
    Am J Med Genet A; 2005 Jan; 132A(3):263-4. PubMed ID: 15523636
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Thirty-two year follow-up of the first patient reported with the Floating-Harbor syndrome.
    Feingold M
    Am J Med Genet A; 2006 Apr; 140(7):782-4. PubMed ID: 16523514
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two patients with Kabuki syndrome presenting with endocrine problems.
    Bereket A; Turan S; Alper G; Comu S; Alpay H; Akalin F
    J Pediatr Endocrinol Metab; 2001 Feb; 14(2):215-20. PubMed ID: 11305802
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Yellow teeth, seizures, and mental retardation: a less severe case of Kohlschütter-Tönz syndrome.
    Haberlandt E; Svejda C; Felber S; Baumgartner S; Günther B; Utermann G; Kotzot D
    Am J Med Genet A; 2006 Feb; 140(3):281-3. PubMed ID: 16411202
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autoimmune disorders in Kabuki syndrome.
    Ming JE; Russell KL; McDonald-McGinn DM; Zackai EH
    Am J Med Genet A; 2005 Jan; 132A(3):260-2. PubMed ID: 15523604
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MOMO syndrome associated with autism: a case report.
    Giunco CT; Moretti-Ferreira D; Silva AE; Rocha SS; Fett-Conte AC
    Genet Mol Res; 2008 Nov; 7(4):1223-5. PubMed ID: 19048502
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polydactyly in a boy with Smith-Magenis syndrome.
    MarianneJensen L; Kirchhoff M
    Clin Dysmorphol; 2005 Oct; 14(4):189-190. PubMed ID: 16155420
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.