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322 related items for PubMed ID: 17380471

  • 1. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia.
    Hatem E, Meriam BR, Walid D, Adenen M, Moez G, Ali S.
    Prenat Diagn; 2007 May; 27(5):471-4. PubMed ID: 17380471
    [Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects.
    López I, Bafalliu JA, Bernabé MC, García F, Costa M, Guillén-Navarro E.
    Prenat Diagn; 2006 Jun; 26(6):577-80. PubMed ID: 16700088
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion.
    Chaabouni M, Martinovic J, Sanlaville D, Attié-Bittach T, Caillat S, Turleau C, Vekemans M, Morichon N.
    Eur J Med Genet; 2006 Jun; 49(6):487-93. PubMed ID: 17142120
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Early onset myoclonic epilepsy and 15q26 microdeletion: observation of the first case.
    Veredice C, Bianco F, Contaldo I, Orteschi D, Stefanini MC, Battaglia D, Lettori D, Guzzetta F, Zollino M.
    Epilepsia; 2009 Jul; 50(7):1810-5. PubMed ID: 19486360
    [Abstract] [Full Text] [Related]

  • 6. Deletion 15q24-26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic development.
    Schlembach D, Zenker M, Trautmann U, Ulmer R, Beinder E.
    Prenat Diagn; 2001 Apr; 21(4):289-92. PubMed ID: 11288119
    [Abstract] [Full Text] [Related]

  • 7. Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome.
    Tamura T, Tohma T, Ohta T, Soejima H, Harada N, Abe K, Niikawa N.
    Clin Dysmorphol; 1993 Apr; 2(2):106-13. PubMed ID: 7506614
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
    Chen CP, Chern SR, Chang TY, Lee CC, Chen LF, Tzen CY, Wang W, Lin CJ, Yang BP, Yang LS.
    Prenat Diagn; 2003 Jan; 23(1):40-3. PubMed ID: 12533811
    [Abstract] [Full Text] [Related]

  • 9. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M, Hwu WL, Kuo SJ, Chen CP, Yin PL, Chang SP, Lee DJ, Chen TH, Wang BT, Lin CC.
    Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
    [Abstract] [Full Text] [Related]

  • 10. Refining the critical region for congenital diaphragmatic hernia on chromosome 15q26 from the study of four fetuses.
    Mosca AL, Pinson L, Andrieux J, Copin H, Bigi N, Puechberty J, Sarda P, Receveur A, Sevestre H, Pigeonnat S, Marle N, Payet M, Ragon C, Rousseau T, Thauvin-Robinet C, Masurel-Paulet A, Schneider A, Laurent N, Sagot P, Mugneret F, Lefort G, Faivre L, Callier P.
    Prenat Diagn; 2011 Sep; 31(9):912-4. PubMed ID: 21706508
    [No Abstract] [Full Text] [Related]

  • 11. Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.
    Slavotinek AM, Moshrefi A, Davis R, Leeth E, Schaeffer GB, Burchard GE, Shaw GM, James B, Ptacek L, Pennacchio LA.
    Eur J Hum Genet; 2006 Sep; 14(9):999-1008. PubMed ID: 16736036
    [Abstract] [Full Text] [Related]

  • 12. Postnatal overgrowth by 15q-trisomy and intrauterine growth retardation by 15q-monosomy due to familial translocation t(13;15): dosage effect of IGF1R?
    Nagai T, Shimokawa O, Harada N, Sakazume S, Ohashi H, Matsumoto N, Obata K, Yoshino A, Murakami N, Murai T, Sakuta R, Niikawa N.
    Am J Med Genet; 2002 Nov 22; 113(2):173-7. PubMed ID: 12407708
    [Abstract] [Full Text] [Related]

  • 13. Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis.
    Stumm M, Klopocki E, Gasiorek-Wiens A, Knoll U, Wirjadi D, Sarioglu N, Wegner RD, Tönnies H.
    Prenat Diagn; 2007 May 22; 27(5):475-8. PubMed ID: 17330228
    [Abstract] [Full Text] [Related]

  • 14. Fryns syndrome phenotype and trisomy 22.
    Ladonne JM, Gaillard D, Carré-Pigeon F, Gabriel R.
    Am J Med Genet; 1996 Jan 02; 61(1):68-70. PubMed ID: 8741922
    [Abstract] [Full Text] [Related]

  • 15. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.
    Chen CP, Su YN, Chen YY, Chern SR, Liu YP, Wu PC, Lee CC, Chen YT, Wang W.
    Taiwan J Obstet Gynecol; 2011 Sep 02; 50(3):345-52. PubMed ID: 22030051
    [Abstract] [Full Text] [Related]

  • 16. Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism.
    Nowaczyk MJ, Ramsay JA, Mohide P, Tomkins DJ.
    Am J Med Genet; 1998 May 26; 77(4):306-9. PubMed ID: 9600741
    [Abstract] [Full Text] [Related]

  • 17. Female pseudohermaphroditism in a fetus with a deletion 9(q22.2q31.1).
    L'Herminé AC, Aboura A, Simon-Bouy B, Robin F, Audibert F, Strouk N, Capron F, Frydman R, Tachdjian G.
    Prenat Diagn; 2002 Aug 26; 22(8):652-5. PubMed ID: 12210571
    [Abstract] [Full Text] [Related]

  • 18. Pulmonary agenesis, microphthalmia, and diaphragmatic defect (PMD): new syndrome or association?
    Berkenstadt M, Lev D, Achiron R, Rosner M, Barkai G.
    Am J Med Genet; 1999 Sep 03; 86(1):6-8. PubMed ID: 10440821
    [Abstract] [Full Text] [Related]

  • 19. Deletion of terminal portion of 6q: report of a case with unusual malformations.
    Shen-Schwarz S, Hill LM, Surti U, Marchese S.
    Am J Med Genet; 1989 Jan 03; 32(1):81-6. PubMed ID: 2705486
    [Abstract] [Full Text] [Related]

  • 20. Association of deletions of the chromosomal region 15q24-ter and diaphragmatic hernia: a new case and discussion of the literature.
    Hengstschläger M, Mittermayer C, Repa C, Drahonsky R, Deutinger J, Bernaschek G.
    Fetal Diagn Ther; 2004 Jan 03; 19(6):510-2. PubMed ID: 15539876
    [Abstract] [Full Text] [Related]

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