BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 30289612)

  • 1. Risk of hepatic neoplasms in Wolf-Hirschhorn syndrome (4p-): Four new cases and review of the literature.
    Battaglia A; Calhoun ARUL; Lortz A; Carey JC
    Am J Med Genet A; 2018 Nov; 176(11):2389-2394. PubMed ID: 30289612
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision.
    Battaglia A; Filippi T; Carey JC
    Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):246-51. PubMed ID: 18932224
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hepatic Malignancy in an Infant with Wolf-Hirschhorn Syndrome.
    Rutter S; Morotti RA; Peterec S; Gallagher PG
    Fetal Pediatr Pathol; 2017 Jun; 36(3):256-262. PubMed ID: 28266898
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Clinical and epilepsy characteristics in Wolf-Hirschhorn syndrome (4p-): A review.
    Paprocka J; KaminiĆ³w K; Yetkin O; Tekturk P; Baykan B; Leiz S; Kluger G; Striano P
    Seizure; 2024 Mar; 116():14-23. PubMed ID: 36526544
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Natural history study of adults with Wolf-Hirschhorn syndrome 2: Patient-reported outcomes study.
    Carey JC; Lortz A; Mendel A; Battaglia A
    Am J Med Genet A; 2021 Jul; 185(7):2065-2069. PubMed ID: 33949758
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Natural history study of adults with Wolf-Hirschhorn syndrome 1: Case series of personally observed 35 individuals.
    Battaglia A; Lortz A; Carey JC
    Am J Med Genet A; 2021 Jun; 185(6):1794-1802. PubMed ID: 33760347
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome.
    Shimizu K; Wakui K; Kosho T; Okamoto N; Mizuno S; Itomi K; Hattori S; Nishio K; Samura O; Kobayashi Y; Kako Y; Arai T; Tsutomu OI; Kawame H; Narumi Y; Ohashi H; Fukushima Y
    Am J Med Genet A; 2014 Mar; 164A(3):597-609. PubMed ID: 24357569
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Wolf-Hirschhorn syndrome: A review and update.
    Battaglia A; Carey JC; South ST
    Am J Med Genet C Semin Med Genet; 2015 Sep; 169(3):216-23. PubMed ID: 26239400
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3.
    South ST; Hannes F; Fisch GS; Vermeesch JR; Zollino M
    Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):270-4. PubMed ID: 18932125
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal phenotype of Wolf-Hirschhorn syndrome: A case series and literature review.
    Tang F; Zeng Y; Wang L; Yin D; Chen L; Xie D; Wang J
    Mol Genet Genomic Med; 2023 Jun; 11(6):e2155. PubMed ID: 36849216
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of Wolf-Hirschhorn syndrome: from ultrasound findings, diagnostic technology to genetic counseling.
    Xing Y; Holder JL; Liu Y; Yuan M; Sun Q; Qu X; Deng L; Zhou J; Yang Y; Guo M; Cheung SW; Sun L
    Arch Gynecol Obstet; 2018 Aug; 298(2):289-295. PubMed ID: 29808250
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome.
    Ho KS; South ST; Lortz A; Hensel CH; Sdano MR; Vanzo RJ; Martin MM; Peiffer A; Lambert CG; Calhoun A; Carey JC; Battaglia A
    J Med Genet; 2016 Apr; 53(4):256-63. PubMed ID: 26747863
    [TBL] [Abstract][Full Text] [Related]  

  • 14. From Wolf-Hirschhorn syndrome to NSD2 haploinsufficiency: a shifting paradigm through the description of a new case and a review of the literature.
    Wiel LC; Bruno I; Barbi E; Sirchia F
    Ital J Pediatr; 2022 May; 48(1):72. PubMed ID: 35550183
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Natural histories of patients with Wolf-Hirschhorn syndrome derived from variable chromosomal abnormalities.
    Yamamoto-Shimojima K; Kouwaki M; Kawashima Y; Itomi K; Momosaki K; Ozasa S; Okamoto N; Yokochi K; Yamamoto T
    Congenit Anom (Kyoto); 2019 Sep; 59(5):169-173. PubMed ID: 30378700
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.
    Zollino M; Orteschi D; Ruiter M; Pfundt R; Steindl K; Cafiero C; Ricciardi S; Contaldo I; Chieffo D; Ranalli D; Acquafondata C; Murdolo M; Marangi G; Asaro A; Battaglia D
    Epilepsia; 2014 Jun; 55(6):849-57. PubMed ID: 24738919
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two cases of hepatic adenomas in patients with Wolf-Hirschhorn syndrome: a new rare complication?
    Prunotto G; Cianci P; Cereda A; Scatigno A; Fossati C; Maitz S; Biondi A; Selicorni A
    Am J Med Genet A; 2013 Jul; 161A(7):1759-62. PubMed ID: 23696331
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Wolf-Hirschhorn syndrome: A case series from India.
    Chaudhry C; Kaur A; Panigrahi I; Kaur A
    Am J Med Genet A; 2020 Dec; 182(12):3048-3051. PubMed ID: 32914558
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three patients with Wolf-Hirschhorn syndrome carrying a satellited chromosome 4p.
    Liang D; Zhou Z; Meng D; Du J; Wen J; Niikawa N; Wu L
    Birth Defects Res A Clin Mol Teratol; 2012 Jul; 94(7):549-52. PubMed ID: 22641563
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 10.