BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 15628630)

  • 21. Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter).
    Chen CP; Lin SP; Chern SR; Lee CC; Chen LF; Chen YJ; Wang W
    Genet Couns; 2006; 17(1):81-5. PubMed ID: 16719283
    [No Abstract]   [Full Text] [Related]  

  • 22. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
    Zaki MS; Kamel AA; El-Ruby M
    Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Interstitial duplication of 20q11.22q13.11: A case report and review of literature.
    Goetzinger L; Starks RD; Dillahunt K; Major H; Nagy JM; Sidhu A
    Mol Genet Genomic Med; 2021 Aug; 9(8):e1755. PubMed ID: 34268909
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Distal 11q monosomy syndrome: a report of two Egyptian sibs with normal parental karyotypes confirmed by molecular cytogenetics.
    Afifi HH; Zaki MS; El-Gerzawy AM; Kayed HF
    Genet Couns; 2008; 19(1):47-58. PubMed ID: 18564501
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
    Girirajan S; Williams S; Garbern J; Nowak N; Hatchwell E; Elsea S
    Clin Genet; 2007 Jul; 72(1):47-58. PubMed ID: 17594399
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Tetrasomy 18p caused by paternal meiotic nondisjunction.
    Eggermann T; Engels H; Apacik C; Moskalonek B; Müller-Navia J; Schwanitz G; Stengel-Rutkowski S
    Eur J Hum Genet; 1997; 5(3):175-7. PubMed ID: 9272743
    [No Abstract]   [Full Text] [Related]  

  • 27. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF; Wyandt H; Huang XL; Milunsky JM
    Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
    Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
    Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases.
    Jedraszak G; Jobic F; Receveur A; Bilan F; Gilbert-Dussardier B; Tiffany B; Missirian C; Willems M; Odent S; Lucas J; Dubourg C; Schaefer E; Scheidecker S; Lespinasse J; Goldenberg A; Guerrot AM; Joly-Helas G; Chambon P; Le Caignec C; David A; Coutton C; Satre V; Vieville G; Amblard F; Harbuz R; Sanlaville D; Till M; Vincent-Delorme C; Colson C; Andrieux J; Naudion S; Toutain J; Rooryck C; de Fréminville B; Prieur F; Daire VC; Amram D; Kleinfinger P; Schulze MB; Raabe-Meyer G; Courage C; Lemke J; Stefanou EG; Loretta T; Emmanouil M; Tzeli SK; Sodowska H; Anderson J; Nandini A; Copin H; Garçon L; Liehr T; Morin G
    Am J Med Genet A; 2024 Apr; 194(4):e63476. PubMed ID: 37974505
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital bile duct anomalies (biliary atresia) and chromosome 22 aneuploidy.
    Allotey J; Lacaille F; Lees MM; Strautnieks S; Thompson RJ; Davenport M
    J Pediatr Surg; 2008 Sep; 43(9):1736-40. PubMed ID: 18779018
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndrome.
    Fryns JP
    Genet Couns; 1998; 9(3):229-30. PubMed ID: 9777347
    [No Abstract]   [Full Text] [Related]  

  • 32. Genetic background of congenital conotruncal heart defects--a study of 45 families.
    Kwiatkowska J; Wierzba J; Aleszewicz-Baranowska J; Ereciński J
    Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Microduplication 22q11.2: a new chromosomal syndrome.
    Portnoï MF
    Eur J Med Genet; 2009; 52(2-3):88-93. PubMed ID: 19254783
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings.
    Laleye A; Alao MJ; Adjagba M; Hans C; Delneste D; Gnamey DK; Ayivi B; Darboux RB
    Genet Couns; 2006; 17(1):35-40. PubMed ID: 16719275
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome.
    Serra G; Giambrone C; Antona V; Cardella F; Carta M; Cimador M; Corsello G; Giuffrè M; Insinga V; Maggio MC; Pensabene M; Schierz IAM; Piro E
    Ital J Pediatr; 2022 Sep; 48(1):170. PubMed ID: 36076277
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mosaic cat eye syndrome in a child with unilateral iris coloboma.
    Hernández-Medrano C; Hidalgo-Bravo A; Villanueva-Mendoza C; Bautista-Tirado T; Apam-Garduño D
    Ophthalmic Genet; 2021 Feb; 42(1):84-87. PubMed ID: 33465332
    [TBL] [Abstract][Full Text] [Related]  

  • 37. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
    Zollino M; Murdolo M; Marangi G; Pecile V; Galasso C; Mazzanti L; Neri G
    Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):257-69. PubMed ID: 18932124
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Further phenotypic delineation of subtelomeric (terminal) 4q deletion with emphasis on intracranial and reproductive anatomy.
    Sills ES; Burns MJ; Parker LD; Carroll LP; Kephart LL; Dyer CS; Papenhausen PR; Davis JG
    Orphanet J Rare Dis; 2007 Feb; 2():9. PubMed ID: 17295911
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Pallister-Killian syndrome: tetrasomy of 12pter-->12p11.22 in a boy with an analphoid, inverted duplicated marker chromosome.
    Huang XL; Isabel de Michelena M; Leon E; Maher TA; McClure R; Milunsky A
    Clin Genet; 2007 Nov; 72(5):434-40. PubMed ID: 17894838
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.
    Murru D; Boccone L; Ristaldi MS; Nucaro AL
    Genet Couns; 2008; 19(4):381-6. PubMed ID: 19239081
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.