181 related articles for article (PubMed ID: 7154050)
1. Interstitial deletion of the long arm of chromosome 5: 46,XX,del(5)(q13q22).
Ohdo S; Madokoro H; Hayakawa K
J Med Genet; 1982 Dec; 19(6):479. PubMed ID: 7154050
[No Abstract] [Full Text] [Related]
2. Interstitial deletion of the long arm of chromosome 5 in a deformed boy: 46,XY,del(5)(q13q15).
Stoll C; Levy J; Roth MP
J Med Genet; 1980 Dec; 17(6):486-7. PubMed ID: 7205434
[TBL] [Abstract][Full Text] [Related]
3. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
McDermott A; Cain R; Howell R
Hum Genet; 1980; 53(3):305-7. PubMed ID: 7372333
[TBL] [Abstract][Full Text] [Related]
4. Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43).
Beemer FA; Klep-de Pater JM; Sepers GJ; Janssen B
Clin Genet; 1985 May; 27(5):515-9. PubMed ID: 4006278
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of the short arm of chromosome 4.
Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
[TBL] [Abstract][Full Text] [Related]
6. Interstitial deletion of the long arm of chromosome 4 in a patient with mental retardation and abnormal phenotype.
del Valle Torrado M; Labarta JD; Migliorini AM
J Med Genet; 1982 Dec; 19(6):477. PubMed ID: 6185682
[No Abstract] [Full Text] [Related]
7. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].
Wilson MG; Towner JW; Coffin GS; Ebbin AJ; Siris E; Brager P
Hum Genet; 1981; 59(4):297-307. PubMed ID: 6949855
[TBL] [Abstract][Full Text] [Related]
8. 4p- syndrome in a girl with translocation t(1;4)(q11;p16)mat.
Stoll C; Pennerath A; Lausecker C
Hum Genet; 1981; 56(3):413-5. PubMed ID: 7239524
[No Abstract] [Full Text] [Related]
9. Complex MCA/MR syndrome associated with interstitial deletion of the long arm of chromosome 6, del(6)(q25.1-->q27).
Vermeesch JR; Fryns JP
Am J Med Genet A; 2003 Jul; 120A(2):299-300. PubMed ID: 12833421
[No Abstract] [Full Text] [Related]
10. The 11q- syndrome with mosaic partial deletion of 11q.
Ishida Y; Watanabe N; Ishihara Y; Matsuda H
Acta Paediatr Jpn; 1992 Dec; 34(6):592-6. PubMed ID: 1285504
[TBL] [Abstract][Full Text] [Related]
11. Simultaneous de novo interstitial deletion of 16q21 and intercalary duplication of 19q in a retarded infant with minor dysmorphic features.
Trautmann U; Pfeiffer RA; Seufert-Satomi U; Tietze HU
J Med Genet; 1993 Apr; 30(4):330-1. PubMed ID: 8487285
[TBL] [Abstract][Full Text] [Related]
12. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32).
Martin-Pont B; Pilczer C; Dandine M; Tamboise A
Ann Genet; 1985; 28(4):251-3. PubMed ID: 3879441
[TBL] [Abstract][Full Text] [Related]
13. A case of de novo interstitial deletion 3q.
Okada N; Hasegawa T; Osawa M; Fukuyama Y
J Med Genet; 1987 May; 24(5):305-8. PubMed ID: 3585947
[TBL] [Abstract][Full Text] [Related]
14. Developmental abnormalities associated with long arm deletion of chromosome No. 6.
Bartoshesky L; Lewis MB; Pashayan HM
Clin Genet; 1978 Jan; 13(1):68-71. PubMed ID: 624189
[TBL] [Abstract][Full Text] [Related]
15. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
Wilson MG; Towner JW; Forsman I; Siris E
Am J Med Genet; 1979; 3(2):155-74. PubMed ID: 474629
[TBL] [Abstract][Full Text] [Related]
16. Three cases of 16q duplication.
Maher ER; Willatt L; Cuthbert G; Chapman C; Hodgson SV
J Med Genet; 1991 Nov; 28(11):801-2. PubMed ID: 1820771
[No Abstract] [Full Text] [Related]
17. Interstitial deletion of band q12 of chromosome 5.
Dudin G; Alexander D; Talj F; Deeb M; Musallam S; Der Kaloustian VM
Clin Genet; 1984 May; 25(5):455-8. PubMed ID: 6723107
[TBL] [Abstract][Full Text] [Related]
18. Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32).
Kroes HY; Tuerlings JH; Hordijk R; Folkers NR; ten Kate LP
J Med Genet; 1994 Feb; 31(2):156-8. PubMed ID: 8182726
[TBL] [Abstract][Full Text] [Related]
19. Deletion of chromosome 2 (p11-p13): case report and review.
Prasher VP; Krishnan VH; Clarke DJ; Maliszewska CT; Corbett JA
J Med Genet; 1993 Jul; 30(7):604-6. PubMed ID: 8411037
[TBL] [Abstract][Full Text] [Related]
20. Terminal deletion(4)(q33) in a male infant.
Stamberg J; Jabs EW; Elias E
Clin Genet; 1982 Feb; 21(2):125-9. PubMed ID: 7083613
[No Abstract] [Full Text] [Related]
[Next] [New Search]