BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 25706929)

  • 1. Diagnosis of 9q22.3 microdeletion syndrome in utero following identification of craniosynostosis, overgrowth, and skeletal anomalies.
    Reichert SC; Zelley K; Nichols KE; Eberhard M; Zackai EH; Martinez-Poyer J
    Am J Med Genet A; 2015 Apr; 167A(4):862-5. PubMed ID: 25706929
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A familial case of overgrowth syndrome caused by a 9q22.3 microdeletion in a mother and daughter.
    Yamada H; Shimura M; Takahashi H; Nara S; Morishima Y; Go S; Miyashita T; Numabe H; Kawashima H
    Eur J Med Genet; 2020 May; 63(5):103872. PubMed ID: 32028043
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay.
    Muller EA; Aradhya S; Atkin JF; Carmany EP; Elliott AM; Chudley AE; Clark RD; Everman DB; Garner S; Hall BD; Herman GE; Kivuva E; Ramanathan S; Stevenson DA; Stockton DW; Hudgins L
    Am J Med Genet A; 2012 Feb; 158A(2):391-9. PubMed ID: 22190277
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Unexpected phenotype in a frameshift mutation of PTCH1.
    Beltrami B; Prada E; Tolva G; Scuvera G; Silipigni R; Graziani D; Bulfamante G; Gervasini C; Marchisio P; Milani D
    Mol Genet Genomic Med; 2020 Jan; 8(1):e987. PubMed ID: 31578813
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome.
    de Ravel TJ; Ameye L; Ballon K; Borghgraef M; Vermeesch JR; Devriendt K
    Eur J Med Genet; 2009; 52(2-3):145-7. PubMed ID: 19233320
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction.
    Chen CP; Ko TM; Huang WC; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):415-8. PubMed ID: 27343326
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Wilms Tumor Associated With the 9q22.3 Microdeletion Syndrome: 2 New Case Reports and a Review of The Literature.
    Cayrol J; Nightingale M; Challis J; Campbell M; Sullivan M; Heloury Y
    J Pediatr Hematol Oncol; 2019 Nov; 41(8):e517-e520. PubMed ID: 30371535
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype.
    Ewing AD; Cheetham SW; McGill JJ; Sharkey M; Walker R; West JA; West MJ; Summers KM
    Am J Med Genet A; 2021 Jul; 185(7):2070-2083. PubMed ID: 33960642
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Prenatal diagnosis of 17q12 microdeletion syndrome in fetal renal abnormalities].
    Jiang YL; Qi QW; Zhou XY; Geng FF; Bai JJ; Hao N; Liu JT
    Zhonghua Fu Chan Ke Za Zhi; 2017 Oct; 52(10):662-668. PubMed ID: 29060963
    [No Abstract]   [Full Text] [Related]  

  • 10. Kagami-Ogata syndrome in a fetus presenting with polyhydramnios, malformations, and preterm delivery: a case report.
    Huang H; Mikami Y; Shigematsu K; Uemura N; Shinsaka M; Iwatani A; Miyake F; Kabe K; Takai Y; Saitoh M; Baba K; Seki H
    J Med Case Rep; 2019 Nov; 13(1):340. PubMed ID: 31753000
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Isolated craniosynostosis: prenatal ultrasound of scaphocephaly with polyhydramnios.
    Huang HW; Lin H; Chang SY; Hsu YH; Hsu TY
    Chang Gung Med J; 2001 Dec; 24(12):816-9. PubMed ID: 11858399
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: report of two cases and review of the literature.
    Yamamoto K; Yoshihashi H; Furuya N; Adachi M; Ito S; Tanaka Y; Masuno M; Chiyo H; Kurosawa K
    Congenit Anom (Kyoto); 2009 Mar; 49(1):8-14. PubMed ID: 19243411
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Kagami-Ogata syndrome: an important differential diagnosis to Beckwith-Wiedemann syndrome.
    Altmann J; Horn D; Korinth D; Eggermann T; Henrich W; Verlohren S
    J Clin Ultrasound; 2020 May; 48(4):240-243. PubMed ID: 31994200
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome.
    Redon R; Baujat G; Sanlaville D; Le Merrer M; Vekemans M; Munnich A; Carter NP; Cormier-Daire V; Colleaux L
    Eur J Hum Genet; 2006 Jun; 14(6):759-67. PubMed ID: 16570072
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome.
    Florisson JM; Mathijssen IM; Dumee B; Hoogeboom JA; Poddighe PJ; Oostra BA; Frijns JP; Koster L; de Klein A; Eussen B; de Vries BB; Swagemakers S; van der Spek PJ; Verkerk AJ
    Am J Med Genet A; 2013 Feb; 161A(2):244-53. PubMed ID: 23303641
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Polyhydramnios, fetal overgrowth, and macrocephaly: prenatal ultrasound findings of Costello syndrome.
    Smith LP; Podraza J; Proud VK
    Am J Med Genet A; 2009 Feb; 149A(4):779-84. PubMed ID: 19288554
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical features of microdeletion 9q22.3 (pat).
    Shimojima K; Adachi M; Tanaka M; Tanaka Y; Kurosawa K; Yamamoto T
    Clin Genet; 2009 Apr; 75(4):384-93. PubMed ID: 19320658
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literature.
    Jones GE; Mousa HA; Rowley H; Houtman P; Vasudevan PC
    Prenat Diagn; 2015 Dec; 35(13):1336-41. PubMed ID: 26429400
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of the 13q-syndrome through three-dimensional ultrasonography: a case report.
    Araujo JĂșnior E; Filho HA; Pires CR; Filho SM
    Arch Gynecol Obstet; 2006 Jul; 274(4):243-5. PubMed ID: 16491370
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.