My NCBI | Sign In
RSS Settings
  • Search:

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

    Results: 1 to 20 of 269

    1.

    Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

    Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J.

    J Med Genet. 1993 Oct;30(10):822-4.PMID: 8230157 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.

    Matsuoka R, Takao A, Kimura M, Imamura S, Kondo C, Joh-o K, Ikeda K, Nishibatake M, Ando M, Momma K.

    Am J Med Genet. 1994 Nov 15;53(3):285-9.PMID: 7856665 [PubMed - indexed for MEDLINE]Related articles

    3.

    Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.

    Momma K, Kondo C, Matsuoka R.

    J Am Coll Cardiol. 1996 Jan;27(1):198-202.PMID: 8522695 [PubMed - indexed for MEDLINE]Related articles

    4.

    Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study.

    Takahashi K, Kido S, Hoshino K, Ogawa K, Ohashi H, Fukushima Y.

    Eur J Pediatr. 1995 Nov;154(11):878-81.PMID: 8582397 [PubMed - indexed for MEDLINE]Related articles

    5.

    Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome.

    Matsuoka R, Kimura M, Scambler PJ, Morrow BE, Imamura S, Minoshima S, Shimizu N, Yamagishi H, Joh-o K, Watanabe S, Oyama K, Saji T, Ando M, Takao A, Momma K.

    Hum Genet. 1998 Jul;103(1):70-80.PMID: 9737780 [PubMed - indexed for MEDLINE]Related articles

    6.

    Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome.

    Momma K, Kondo C, Matsuoka R, Takao A.

    Am J Cardiol. 1996 Sep 1;78(5):591-4.PMID: 8806353 [PubMed - indexed for MEDLINE]Related articles

    7.

    Anatomic patterns of conotruncal defects associated with deletion 22q11.

    Marino B, Digilio MC, Toscano A, Anaclerio S, Giannotti A, Feltri C, de Ioris MA, Angioni A, Dallapiccola B.

    Genet Med. 2001 Jan-Feb;3(1):45-8.PMID: 11339377 [PubMed - indexed for MEDLINE]Related articles

    8.

    Genetic basis of DiGeorge and velocardiofacial syndromes.

    Driscoll DA.

    Curr Opin Pediatr. 1994 Dec;6(6):702-6. Review.PMID: 7849818 [PubMed - indexed for MEDLINE]Related articles

    9.

    Size of 22q deletions in four previously reported patients with conotruncal anomaly face syndrome.

    Pierpont JW, Erickson RP, Thompson FH, Yang JM.

    Clin Genet. 1996 Dec;50(6):545-7.PMID: 9147896 [PubMed - indexed for MEDLINE]Related articles

    10.

    Tetralogy of Fallot associated with chromosome 22q11 deletion.

    Momma K, Kondo C, Ando M, Matsuoka R, Takao A.

    Am J Cardiol. 1995 Sep 15;76(8):618-21. No abstract available. PMID: 7677092 [PubMed - indexed for MEDLINE]Related articles

    11.

    Chromosomes 22q11 deletion syndrome: an update and review for the primary pediatrician.

    Thomas JA, Graham JM Jr.

    Clin Pediatr (Phila). 1997 May;36(5):253-66. Review.PMID: 9152551 [PubMed - indexed for MEDLINE]Related articles

    12.

    Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.

    Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS, Shprintzen RJ, Baldini A.

    Am J Med Genet. 1995 Jul 3;57(3):514-22.PMID: 7677167 [PubMed - indexed for MEDLINE]Related articles

    13.

    Frequency of 22q11 deletions in patients with conotruncal defects.

    Goldmuntz E, Clark BJ, Mitchell LE, Jawad AF, Cuneo BF, Reed L, McDonald-McGinn D, Chien P, Feuer J, Zackai EH, Emanuel BS, Driscoll DA.

    J Am Coll Cardiol. 1998 Aug;32(2):492-8.PMID: 9708481 [PubMed - indexed for MEDLINE]Related articles

    14.

    DNA fluorescent probes for diagnosis of velocardiofacial and related syndromes.

    Crifasi PA, Michels VV, Driscoll DJ, Jalal SM, Dewald GW.

    Mayo Clin Proc. 1995 Dec;70(12):1148-53.PMID: 7490915 [PubMed - indexed for MEDLINE]Related articles

    15.

    CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.

    Sergi C, Serpi M, Müller-Navia J, Schnabel PA, Hagl S, Otto HF, Ulmer HE.

    Pathologica. 1999 Jun;91(3):166-72. Review.PMID: 10536461 [PubMed - indexed for MEDLINE]Related articles

    16.

    Phenotypic discordance in monozygotic twins with 22q11.2 deletion.

    Yamagishi H, Ishii C, Maeda J, Kojima Y, Matsuoka R, Kimura M, Takao A, Momma K, Matsuo N.

    Am J Med Genet. 1998 Jul 24;78(4):319-21.PMID: 9714432 [PubMed - indexed for MEDLINE]Related articles

    17.

    Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.

    Alikaşifoğlu M, Malkoç N, Ceviz N, Ozme S, Uludoğan S, Tunçbilek E.

    Turk J Pediatr. 2000 Jul-Sep;42(3):215-8.PMID: 11105620 [PubMed - indexed for MEDLINE]Related articles

    18.

    Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.

    Webber SA, Hatchwell E, Barber JC, Daubeney PE, Crolla JA, Salmon AP, Keeton BR, Temple IK, Dennis NR.

    J Pediatr. 1996 Jul;129(1):26-32.PMID: 8757559 [PubMed - indexed for MEDLINE]Related articles

    19.

    Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.

    Goldmuntz E, Driscoll D, Budarf ML, Zackai EH, McDonald-McGinn DM, Biegel JA, Emanuel BS.

    J Med Genet. 1993 Oct;30(10):807-12.PMID: 7901419 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients.

    McDonald-McGinn DM, LaRossa D, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Wang P, Solot C, Schultz P, Lynch D, Bingham P, Keenan G, Weinzimer S, Ming JE, Driscoll D, Clark BJ 3rd, Markowitz R, Cohen A, Moshang T, Pasquariello P, Randall P, Emanuel BS, Zackai EH.

    Genet Test. 1997;1(2):99-108.PMID: 10464633 [PubMed - indexed for MEDLINE]Related articles

    Supplemental Content

    Filter your results:

    Find related data

    Recent activity