66 related articles for article (PubMed ID: 10636744)
1. Clinical and molecular findings in a patient with a deletion on the long arm of chromosome 12.
Brady AF; Elsawi MM; Jamieson CR; Marks K; Jeffery S; Patton MA; Murtaza L; Savage MO
J Med Genet; 1999 Dec; 36(12):939-41. PubMed ID: 10636744
[No Abstract] [Full Text] [Related]
2. Chromosome 13 long arm interstitial deletion associated with features of Noonan phenotype.
Onufer CN; Stephan MJ; Thuline HC; Char F
Ann Genet; 1987; 30(4):236-9. PubMed ID: 3501267
[TBL] [Abstract][Full Text] [Related]
3. Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12.
Brady AF; Jamieson CR; van der Burgt I; Crosby A; van Reen M; Kremer H; Mariman E; Patton MA; Jeffery S
Eur J Hum Genet; 1997; 5(5):336-7. PubMed ID: 9412792
[No Abstract] [Full Text] [Related]
4. Deletion of the proximal long arm of chromosome 3 in an infant with features of Turner syndrome.
Jenkins MB; Stang HJ; Davis E; Boyd L
Ann Genet; 1985; 28(1):42-4. PubMed ID: 3874587
[TBL] [Abstract][Full Text] [Related]
5. Exclusion of 22q11 deletion in Noonan syndrome with tetralogy of Fallot.
Digilio MC; Marino B; Giannotti A; Dallapiccola B
Am J Med Genet; 1996 Apr; 62(4):413-4. PubMed ID: 8723074
[No Abstract] [Full Text] [Related]
6. Ullrich-Turner syndrome associated with interstitial deletion of Xp11.4 leads to p22.31.
Wilson MG; Modebe O; Towner JW; Frasier SD; Lin MS
Am J Med Genet; 1983 Mar; 14(3):567-76. PubMed ID: 6859107
[TBL] [Abstract][Full Text] [Related]
7. Case of interstitial 12q deletion in association with Wilms tumor.
Rapley EA; Hargrave D; Persinguhe N; Barfoot R; Moore I; Radford M; Stratton MR; Rahman N; Pritchard-Jones K
Am J Med Genet; 2001 Dec; 104(3):246-9. PubMed ID: 11754052
[TBL] [Abstract][Full Text] [Related]
8. Small terminal 10q26 deletion in a male patient with Noonan-like stigmata: diagnosis by cytogenetic and FISH analysis.
Lukusa T; Smeets E; Vermeesch JR; Fryns JP
Genet Couns; 2002; 13(4):417-25. PubMed ID: 12558112
[TBL] [Abstract][Full Text] [Related]
9. The human ribosomal protein L6 gene in a critical region for Noonan syndrome.
Kenmochi N; Yoshihama M; Higa S; Tanaka T
J Hum Genet; 2000; 45(5):290-3. PubMed ID: 11043511
[TBL] [Abstract][Full Text] [Related]
10. Are Noonan syndrome and Noonan-like/multiple giant cell lesion syndrome distinct entities?
Bertola DR; Kim CA; Pereira AC; Mota GF; Krieger JE; Vieira IC; Valente M; Loreto MR; Magalhães RP; Gonzalez CH
Am J Med Genet; 2001 Jan; 98(3):230-4. PubMed ID: 11169560
[TBL] [Abstract][Full Text] [Related]
11. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
[TBL] [Abstract][Full Text] [Related]
12. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
[TBL] [Abstract][Full Text] [Related]
13. Deletions at chromosome 2q and 12p are early and frequent molecular alterations in bronchial epithelium and NSCLC of long-term smokers.
Grepmeier U; Dietmaier W; Merk J; Wild PJ; Obermann EC; Pfeifer M; Hofstaedter F; Hartmann A; Woenckhaus M
Int J Oncol; 2005 Aug; 27(2):481-8. PubMed ID: 16010431
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment.
Gould DB; Jaafar MS; Addison MK; Munier F; Ritch R; MacDonald IM; Walter MA
BMC Med Genet; 2004 Jun; 5():17. PubMed ID: 15219231
[TBL] [Abstract][Full Text] [Related]
15. A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.
Harvard C; Malenfant P; Koochek M; Creighton S; Mickelson EC; Holden JJ; Lewis ME; Rajcan-Separovic E
Clin Genet; 2005 Apr; 67(4):341-51. PubMed ID: 15733271
[TBL] [Abstract][Full Text] [Related]
16. [Noonan syndrome].
Suzuki Y
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):218-9. PubMed ID: 11057203
[No Abstract] [Full Text] [Related]
17. Frequent loss of copy number on the long arm of chromosome 21 in human esophageal squamous cell carcinoma.
Mayama T; Fukushige S; Shineha R; Nishihira T; Satomi S; Horii A
Int J Oncol; 2000 Aug; 17(2):245-52. PubMed ID: 10891531
[TBL] [Abstract][Full Text] [Related]
18. Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.
Cargile CB; Goh DL; Goodman BK; Chen XN; Korenberg JR; Semenza GL; Thomas GH
Am J Med Genet; 2002 Apr; 109(2):133-8. PubMed ID: 11977162
[TBL] [Abstract][Full Text] [Related]
19. Interstitial deletions at the long arm of chromosome 13 may be as common as monosomies in multiple myeloma. A genotypic study.
Nomdedéu JF; Lasa A; Ubeda J; Saglio G; Bellido M; Casas S; Carnicer MJ; Aventín A; Sureda A; Sierra J; Baiget M
Haematologica; 2002 Aug; 87(8):828-35. PubMed ID: 12161359
[TBL] [Abstract][Full Text] [Related]
20. Williams-Beuren syndrome: determination of deletion size using quantitative real-time PCR.
Schubert C; Laccone F
Int J Mol Med; 2006 Nov; 18(5):799-806. PubMed ID: 17016608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]