111 related articles for article (PubMed ID: 15756225)
1. Genetic analyses in two extended families with deletion 22q11 syndrome: importance of extracardiac manifestations.
Shooner KA; Rope AF; Hopkin RJ; Andelfinger GU; Benson DW
J Pediatr; 2005 Mar; 146(3):382-7. PubMed ID: 15756225
[TBL] [Abstract][Full Text] [Related]
2. Otolaryngological manifestations of velocardiofacial syndrome: a retrospective review of 35 patients.
Ford LC; Sulprizio SL; Rasgon BM
Laryngoscope; 2000 Mar; 110(3 Pt 1):362-7. PubMed ID: 10718420
[TBL] [Abstract][Full Text] [Related]
3. Genetic background of congenital conotruncal heart defects--a study of 45 families.
Kwiatkowska J; Wierzba J; Aleszewicz-Baranowska J; Ereciński J
Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
[TBL] [Abstract][Full Text] [Related]
4. Children with a 22q11 deletion versus children with a speech-language impairment and learning disability: behavior during primary school age.
Swillen A; Devriendt K; Ghesquière P; Fryns JP
Genet Couns; 2001; 12(4):309-17. PubMed ID: 11837599
[TBL] [Abstract][Full Text] [Related]
5. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
Beauchesne LM; Warnes CA; Connolly HM; Ammash NM; Grogan M; Jalal SM; Michels VV
J Am Coll Cardiol; 2005 Feb; 45(4):595-8. PubMed ID: 15708709
[TBL] [Abstract][Full Text] [Related]
6. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
Qin YF; Yang JB; Xie CH; Shao J; Zhao ZY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):284-7. PubMed ID: 17557238
[TBL] [Abstract][Full Text] [Related]
7. A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome.
Hassed SJ; Hopcus-Niccum D; Zhang L; Li S; Mulvihill JJ
Clin Genet; 2004 May; 65(5):400-4. PubMed ID: 15099348
[TBL] [Abstract][Full Text] [Related]
8. [Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations].
Eirís-Puñal J; Iglesias-Meleiro JM; Blanco-Barca MO; Fuster-Siebert M; Barros-Angueira F; Ansede A; Castro-Gago M
Rev Neurol; 2003 Oct 1-15; 37(7):601-7. PubMed ID: 14582013
[TBL] [Abstract][Full Text] [Related]
9. [22q11 deletion syndrome: an expanding phenotype].
Moreno Izco F; Zuazo Zamalloa E; González Alvaredo S; Bereciartu Irastorza P
Neurologia; 2009; 24(1):69-71. PubMed ID: 19214819
[TBL] [Abstract][Full Text] [Related]
10. Molecular characterization of 22q11 deletion in a three-generation family with maternal transmission.
Iascone MR; Vittorini S; Sacchelli M; Spadoni I; Simi P; Giusti S
Am J Med Genet; 2002 Apr; 108(4):319-21. PubMed ID: 11920838
[TBL] [Abstract][Full Text] [Related]
11. Associated anomalies in asymmetric crying facies and 22q11 deletion.
Akcakus M; Ozkul Y; Gunes T; Kurtoglu S; Cetin N; Kisaarslan AP; Dundar M
Genet Couns; 2003; 14(3):325-30. PubMed ID: 14577677
[TBL] [Abstract][Full Text] [Related]
12. Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.
Kang SH; Scheffer A; Ou Z; Li J; Scaglia F; Belmont J; Lalani SR; Roeder E; Enciso V; Braddock S; Buchholz J; Vacha S; Chinault AC; Cheung SW; Bacino CA
Clin Genet; 2007 Oct; 72(4):329-38. PubMed ID: 17850629
[TBL] [Abstract][Full Text] [Related]
13. Facial features in children with the 22q11 deletion syndrome.
Oskarsdóttir S; Holmberg E; Fasth A; Strömland K
Acta Paediatr; 2008 Aug; 97(8):1113-7. PubMed ID: 18482168
[TBL] [Abstract][Full Text] [Related]
14. 22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay.
Cusmano-Ozog K; Manning MA; Hoyme HE
Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):393-8. PubMed ID: 17926345
[TBL] [Abstract][Full Text] [Related]
15. Transmitted cytogenetic abnormalities in patients with mental retardation: pathogenic or normal variants?
Bisgaard AM; Kirchhoff M; Nielsen JE; Brandt C; Hove H; Jepsen B; Jensen T; Ullmann R; Skovby F
Eur J Med Genet; 2007; 50(4):243-55. PubMed ID: 17531565
[TBL] [Abstract][Full Text] [Related]
16. Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney.
Wieser R; Fritz B; Ullmann R; Müller I; Galhuber M; Storlazzi CT; Ramaswamy A; Christiansen H; Shimizu N; Rehder H
Hum Mutat; 2005 Aug; 26(2):78-83. PubMed ID: 15957176
[TBL] [Abstract][Full Text] [Related]
17. 1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.
Alberti A; Romano C; Falco M; Calì F; Schinocca P; Galesi O; Spalletta A; Di Benedetto D; Fichera M
Clin Genet; 2007 Feb; 71(2):177-82. PubMed ID: 17250668
[TBL] [Abstract][Full Text] [Related]
18. [A study on the occurrence of the deletion 22q11.2 in patients affected with a psychiatric disease].
Pawłowska B; Tomankiewicz-Zawadzka A; Ilnicka A; Bogdanowicz J; Wciórka J; Szafrański T; Woźniak P; Meder J; Szaniawska-Bartnicka A; Zdzienicka E; Szirkowiec W; Zaremba J
Psychiatr Pol; 2007; 41(2):251-60. PubMed ID: 17598434
[TBL] [Abstract][Full Text] [Related]
19. Clinical, anatomopathological and genetic pattern of 10 patients with cervical aortic arch.
Baravelli M; Borghi A; Rogiani S; Preda L; Quattrociocchi M; Fantoni C; Crupi G; Tiraboschi R
Int J Cardiol; 2007 Jan; 114(2):236-40. PubMed ID: 16781789
[TBL] [Abstract][Full Text] [Related]
20. FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II.
Gentile M; De Sanctis S; Cariola F; Spezzi T; Di Carlo A; Tontoli F; Lista F; Buonadonna AL
Eur J Med Genet; 2005; 48(1):33-9. PubMed ID: 15953404
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
