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191 related items for PubMed ID: 1493641

  • 1. The Wolf-Hirschhorn syndrome in fetuses.
    Tachdjian G, Fondacci C, Tapia S, Huten Y, Blot P, Nessmann C.
    Clin Genet; 1992 Dec; 42(6):281-7. PubMed ID: 1493641
    [Abstract] [Full Text] [Related]

  • 2. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
    Dietze I, Fritz B, Huhle D, Simoens W, Piecha E, Rehder H.
    Fetal Diagn Ther; 2004 Dec; 19(3):251-60. PubMed ID: 15067236
    [Abstract] [Full Text] [Related]

  • 3. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF.
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [Abstract] [Full Text] [Related]

  • 4. [Wolf-Hirschhorn syndrome].
    Heljić S, Catibusić F, Dozić M, Mackić M.
    Med Arh; 2004 Jun; 58(5):318-20. PubMed ID: 15628261
    [Abstract] [Full Text] [Related]

  • 5. [Prenatal diagnosis and genetic analysis of two fetuses with Wolf-Hirschhorn syndrome].
    Li F, Wu A, Xie X, Ma M, Tang J, Tang S, Tan W, Yin W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Oct 10; 41(10):1201-1205. PubMed ID: 39344614
    [Abstract] [Full Text] [Related]

  • 6. Wolf-Hirschhorn syndrome due to a 3:1 segregation of a maternal balanced t(4;15)(p16.3;q11) translocation.
    Zimmermann-Bär U, Stallmach T, Riegel M, Wiedemann U, Fauchère JC, Binkert F, Kotzot D.
    Prenat Diagn; 2000 Oct 10; 20(10):847-50. PubMed ID: 11038468
    [Abstract] [Full Text] [Related]

  • 7. Prenatal detection of congenital hypospadias in the Wolf-Hirschhorn (4p-) syndrome.
    Viñals F, Sepulveda W, Selman E.
    Prenat Diagn; 1994 Dec 10; 14(12):1166-9. PubMed ID: 7899285
    [Abstract] [Full Text] [Related]

  • 8. Distal 4p microdeletion in a case of Wolf-Hirschhorn syndrome with congenital diaphragmatic hernia.
    Casaccia G, Mobili L, Braguglia A, Santoro F, Bagolan P.
    Birth Defects Res A Clin Mol Teratol; 2006 Mar 10; 76(3):210-3. PubMed ID: 16498629
    [Abstract] [Full Text] [Related]

  • 9. Prenatal sonographic patterns in six cases of Wolf-Hirschhorn (4p-) syndrome.
    Boog G, Le Vaillant C, Collet M, Dupré PF, Parent P, Bongain A, Benoit B, Trastour C.
    Fetal Diagn Ther; 2004 Mar 10; 19(5):421-30. PubMed ID: 15305099
    [Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).
    Kohlschmidt N, Zielinski J, Brude E, Schäfer D, Olert J, Hallermann C, Coerdt W, Arnemann J.
    Prenat Diagn; 2000 Feb 10; 20(2):152-5. PubMed ID: 10694689
    [Abstract] [Full Text] [Related]

  • 11. Early diagnosis of Wolf-Hirschhorn syndrome triggered by a life-threatening event: congenital diaphragmatic hernia.
    van Dooren MF, Brooks AS, Hoogeboom AJ, van den Hoonaard TL, de Klein JE, Wouters CH, Tibboel D.
    Am J Med Genet A; 2004 Jun 01; 127A(2):194-6. PubMed ID: 15108210
    [Abstract] [Full Text] [Related]

  • 12. [Identification of a critical region on chromosome 4p16.3 for Wolf-Hirschhorn syndrome-associated fetal growth retardation].
    Zheng W, Chen B, Yin Z, Huang X, Liang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul 10; 37(7):731-735. PubMed ID: 32619252
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital diaphragmatic hernia, cystic hygroma and IUGR.
    Basgul A, Kavak ZN, Akman I, Basgul A, Gokaslan H, Elcioglu N.
    Clin Exp Obstet Gynecol; 2006 Jul 10; 33(2):105-6. PubMed ID: 16903248
    [Abstract] [Full Text] [Related]

  • 14. De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia.
    Chen CP, Chern SR, Lee CC, Chen WL, Chen MH, Chang KM.
    J Med Genet; 1998 Dec 10; 35(12):1050-3. PubMed ID: 9863609
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.
    Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2017 Dec 10; 56(6):821-826. PubMed ID: 29241927
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of monosomy 4p14-->pter and trisomy 11q25-->qter: clinical presentations and outcomes.
    Peng HH, Wang TH, Chao AS, Chang YL, Chang SD, Soong YK.
    Prenat Diagn; 2005 Dec 10; 25(12):1133-7. PubMed ID: 16231301
    [Abstract] [Full Text] [Related]

  • 17. Prenatal diagnosis and fetal pathology of partial trisomy 20P-monosomy 4P resulting from paternal translocation.
    Vamos E, Pratola D, Van Regemorter N, Freund M, Flament-Durand J, Rodesch F.
    Prenat Diagn; 1985 Dec 10; 5(3):209-14. PubMed ID: 2410900
    [Abstract] [Full Text] [Related]

  • 18. [Study on clinical features and diagnostic methods of prenatal Wolf-Hirschhorn syndrome].
    Wang Y, Chen X, Xue H, Chen L, Chen M, Huang H, He D, Xu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Aug 10; 38(8):735-739. PubMed ID: 34365613
    [Abstract] [Full Text] [Related]

  • 19. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ, Huang ZY, Wu WQ, Zhao Q, Jiang HY, Xie JS.
    Zhonghua Er Ke Za Zhi; 2012 Jun 10; 50(6):460-4. PubMed ID: 22931946
    [Abstract] [Full Text] [Related]

  • 20. 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 10; 11(6):e2155. PubMed ID: 36849216
    [Abstract] [Full Text] [Related]

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