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: 3611633)

  • 1. The brain in partial trisomy 18: a case report.
    Novotny EJ; Urich H
    J Child Neurol; 1987 Jul; 2(3):194-7. PubMed ID: 3611633
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A case report: corpus callosum dysgenesis, microcephaly, infantile spasm, cleft lip-palate, exophthalmos and psychomotor retardation.
    Tütüncüoglu S; Ozkinay F; Genel F; Uran N; Ozgür T
    Clin Genet; 1996 Apr; 49(4):220-2. PubMed ID: 8828990
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature.
    Simpson J; Zellweger H
    J Med Genet; 1977 Apr; 14(2):124-7. PubMed ID: 853318
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Monosomy and trisomy of 15q24-qter with cleft lip and palate.
    Abe A; Hatano Y; Kurita K; Nakano M; Shimizu M; Yokoi T; Sugiyama N
    Int J Oral Maxillofac Surg; 2008 May; 37(5):487-90. PubMed ID: 18262763
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
    Sanchez O; Yunis JJ; Escobar JI
    Humangenetik; 1974 Apr; 22(1):59-65. PubMed ID: 4134840
    [No Abstract]   [Full Text] [Related]  

  • 6. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
    Riegel M; Schinzel A
    Am J Med Genet; 2002 Jul; 111(1):76-80. PubMed ID: 12124740
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization.
    Jelin A; Perry H; Hogue J; Oberoi S; Cotter PD; Klein OD
    J Craniofac Surg; 2010 Sep; 21(5):1376-9. PubMed ID: 20856024
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Orofacial findings and dental treatment in an 8-year-old patient with trisomy 18: a case report.
    de Queiroz AM; Raffaini MS; de Camargo LM; de Pina Neto JM; Melo DG; Silva RA
    J Dent Child (Chic); 2007; 74(1):67-72. PubMed ID: 18430358
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Free proximal trisomy 21 without the Down syndrome.
    Park JP; Wurster-Hill DH; Andrews PA; Cooley WC; Graham JM
    Clin Genet; 1987 Nov; 32(5):342-8. PubMed ID: 2446809
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Large duplication 4q25-q34 with mild clinical effect.
    Elghezal H; Sendi HS; Monastiri K; Lapierre JM; Romdhane SI; Mougou S; Saad A
    Ann Genet; 2004; 47(4):419-22. PubMed ID: 15581841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GROUP B/D TRANSLOCATION CHROMOSOME IN A CASE WITH STIGMATA OF THE D TRISOMY.
    WALLACE C; ANDERSON IF
    S Afr Med J; 1964 May; 38():352-4. PubMed ID: 14153715
    [No Abstract]   [Full Text] [Related]  

  • 12. Tetrasomy 21 pter→q21.3 due to an extra +dic(21;21)mat in a severely psychomotor-retarded female patient without Down syndrome phenotype.
    Takano T; Nakabayashi K; Ota H; Arai Y; Kamura H; Hata K
    Eur J Med Genet; 2020 Apr; 63(4):103824. PubMed ID: 31830537
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation.
    Manolakos E; Vetro A; Kefalas K; Thomaidis L; Aperis G; Sotiriou S; Kitsos G; Merkas M; Sifakis S; Papoulidis I; Liehr T; Zuffardi O; Petersen MB
    Am J Med Genet A; 2011 Jun; 155A(6):1476-82. PubMed ID: 21567918
    [No Abstract]   [Full Text] [Related]  

  • 14. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
    Frankova YE; Holenova H; Braulke I
    Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bilateral Cleft Lip and Palate in Ring Chromosome 7 Syndrome: A Case Report and Review of Clinical Characteristics.
    Bangun K; Kreshanti P; Tania V; Ariani Aswin Y; Menna C; Aurino L
    Cleft Palate Craniofac J; 2024 Mar; 61(3):527-533. PubMed ID: 36624583
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A case of Patau syndrome. Fetal heart defect and lip-jaw-palate cleft as indicators].
    Küffer E; Asseryanis E; Eppel W; Schurz B; Reinold E
    Ultraschall Med; 1994 Aug; 15(4):217-8. PubMed ID: 7973594
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trisomy 22 in a liveborn infant with multiple congenital anomalies.
    McPherson E; Stetka DG
    Am J Med Genet; 1990 May; 36(1):11-4. PubMed ID: 2333899
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Supernumerary marker chromosome in a child with microcephaly and mental retardation.
    Sheth F; Andrieux J; Sheth J
    Indian Pediatr; 2010 Mar; 47(3):277-9. PubMed ID: 20371896
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tertiary trisomy (22q11q),47,+der(22),t(11;22).
    Biederman BM; Lin CC; Lowry RB; Somerville R
    Hum Genet; 1980 Feb; 53(2):173-7. PubMed ID: 7358384
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A, 1;6, translocation associated with congenital glaucoma and cleft lip and palate.
    Tinning S; Jacobsen P; Mikkelsen M
    Hum Hered; 1975; 25(6):453-60. PubMed ID: 1225819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.