BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 7815448)

  • 1. "CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency?
    Lipson A; Emanuel B; Colley P; Fagan K; Driscoll DA
    J Med Genet; 1994 Sep; 31(9):741. PubMed ID: 7815448
    [No Abstract]   [Full Text] [Related]  

  • 2. CATCH 22 Syndrome.
    Yonehara Y; Nakatsuka T; Ichioka S; Sasaki N; Kobayashi T
    J Craniofac Surg; 2002 Sep; 13(5):623-6. PubMed ID: 12218787
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 10536461
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DiGeorge syndrome: part of CATCH 22.
    Wilson DI; Burn J; Scambler P; Goodship J
    J Med Genet; 1993 Oct; 30(10):852-6. PubMed ID: 8230162
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Study of CATCH 22: genetic aspects].
    Antonenko VG; Ivanov VI; Konstantinova LM; Levina LIa; Mglinets VA
    Vestn Ross Akad Med Nauk; 2000; (5):46-50. PubMed ID: 10881663
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CATCHing a break on 22.
    Glover TW
    Nat Genet; 1995 Jul; 10(3):257-8. PubMed ID: 7670460
    [No Abstract]   [Full Text] [Related]  

  • 7. [Teleradiographic analysis of velopharyngeal insufficiency in CATCH 22 association].
    Houze de L'Aulnoit S; Martinot V; Breviere GM; Kulik JF; Pellerin P
    Ann Chir Plast Esthet; 1999 Oct; 44(5):525-30. PubMed ID: 10609375
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CATCH 22: a possible cause of congenital unilateral facial nerve palsy.
    Ehara H; Hara T; Takeshita K
    Eur J Pediatr; 1997 Sep; 156(9):739. PubMed ID: 9296543
    [No Abstract]   [Full Text] [Related]  

  • 9. 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. PubMed ID: 7490915
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [CATCH 22].
    Matsuo N; Yamagishi H
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):150-3. PubMed ID: 11057175
    [No Abstract]   [Full Text] [Related]  

  • 11. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
    Von Beust G; Bartmus D; Bartels I
    Genet Couns; 1998; 9(3):223-7. PubMed ID: 9777346
    [No Abstract]   [Full Text] [Related]  

  • 12. Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.
    Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
    Dev Med Child Neurol; 2002 Jan; 44(1):44-50. PubMed ID: 11811651
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 42(3):215-8. PubMed ID: 11105620
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC; Marino B; Bagolan P; Giannotti A; Dallapiccola B
    J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 53(3):285-9. PubMed ID: 7856665
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening of patients at risk for 22q11 deletion.
    Barisić I; Morozin Pohovski L; Petković I; Cvetko Z; Stipancić G; Bagatin M
    Coll Antropol; 2008 Mar; 32(1):165-9. PubMed ID: 18494202
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microdeletion 22q11 in complex cardiovascular malformations.
    Mehraein Y; Wippermann CF; Michel-Behnke I; Nhan Ngo TK; Hillig U; Giersberg M; Aulepp U; Barth H; Fritz B; Rehder H
    Hum Genet; 1997 Apr; 99(4):433-42. PubMed ID: 9099830
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Microdeletion of the chromosome 22q11 in children: apropos of a series of 49 patients].
    Levy-Mozziconacci A; Lacombe D; Leheup B; Wernert F; Rouault F; Philip N
    Arch Pediatr; 1996 Aug; 3(8):761-8. PubMed ID: 8998528
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [CATCH-22: a microdeletion of chromosome 22 behind the polymorphous syndrome].
    Somer M; Ignatius J; Vehmanen P; Keinänen M; Haapanen ML
    Duodecim; 1997; 113(12):1115-22. PubMed ID: 11466836
    [No Abstract]   [Full Text] [Related]  

  • 20. [Clinical features and molecular diagnosis of three patients with DiGeorge anomaly].
    Sun JQ; Wang LS; Qi CH; Ying WJ; Guo XH; Liu DR; Hui XY; Liu F; Cao Y; Luo FH; Wang XC
    Zhonghua Er Ke Za Zhi; 2012 Dec; 50(12):944-7. PubMed ID: 23324155
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.