188 related articles for article (PubMed ID: 912940)
1. 7q deletion syndrome (7q32 leads to 7qter).
Harris EL; Wappner RS; Palmer CG; Hall B; Dinno N; Seashore MR; Breg WR
Clin Genet; 1977 Oct; 12(4):233-8. PubMed ID: 912940
[TBL] [Abstract][Full Text] [Related]
2. Brief clinical report: cebocephaly-holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter leads to q32:)].
Schwartz S; Meekins J; Panny SR; Sun CC; Cohen MM
Am J Med Genet; 1983 May; 15(1):141-4. PubMed ID: 6859113
[TBL] [Abstract][Full Text] [Related]
3. A new syndrome of proximal deletion of the long arm of chromosome 1: 1q21-23 leads to 1q25.
Taysi K; Sekhon GS; Hillman RE
Am J Med Genet; 1982 Dec; 13(4):423-30. PubMed ID: 7158642
[No Abstract] [Full Text] [Related]
4. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
Young RS; Palmer CG; Bender HA; Weaver DD; Hodes ME
Am J Med Genet; 1982 May; 12(1):103-7. PubMed ID: 7091193
[No Abstract] [Full Text] [Related]
5. [Interstitial deletion of the long arm of one 11 chromosome].
Taillemite JL; Morlier BG; Roux C
Ann Genet; 1975 Mar; 18(1):61-3. PubMed ID: 1080039
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Deletion of 11q: report of two cases and a review.
Larson SA; Yeatman GW; Riccardi VM
Birth Defects Orig Artic Ser; 1976; 12(5):125-30. PubMed ID: 953212
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Interstitial deletion of long arm of chromosome 13.
Carnevale A; Frias S; Alcantar R
Ann Genet; 1984; 27(1):49-52. PubMed ID: 6609673
[TBL] [Abstract][Full Text] [Related]
10. 46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit.
Fryns JP; Kleczkowska A; Decock P; Massa G; van den Berghe H
Ann Genet; 1992; 35(4):234-6. PubMed ID: 1296522
[TBL] [Abstract][Full Text] [Related]
11. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3).
Copelli S; del Rey G; Heinrich J; Coco R
Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102
[TBL] [Abstract][Full Text] [Related]
12. The 18p- syndrome. Report of five cases.
Zumel RM; Darnaude MT; Delicado A; Diaz de Bustamante A; de Torres ML; López-Pájares I
Ann Genet; 1989; 32(3):160-3. PubMed ID: 2817777
[TBL] [Abstract][Full Text] [Related]
13. Langer-Giedion syndrome with interstitial 8q-deletion.
Zabel BU; Baumann WA
Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
[TBL] [Abstract][Full Text] [Related]
14. Chromosome 6q- and associated malformations.
Liberfarb RM; Atkins L; Holmes LB
Ann Genet; 1978 Dec; 21(4):223-5. PubMed ID: 314259
[TBL] [Abstract][Full Text] [Related]
15. Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant.
Gillar PJ; Kaye CI; Ryan SG; Moore CM
Am J Med Genet; 1992 Sep; 44(2):138-41. PubMed ID: 1456281
[TBL] [Abstract][Full Text] [Related]
16. Partial trisomy 7q in two siblings.
Klasen M; Schmid M; Hansmann I; Grimm T
Ann Genet; 1983; 26(2):100-2. PubMed ID: 6604481
[TBL] [Abstract][Full Text] [Related]
17. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
Pai GS; Thomas GH; Leonard CO; Ward JC; Valle DL; Pyeritz RE
Johns Hopkins Med J; 1979 Oct; 145(4):162-9. PubMed ID: 491337
[No Abstract] [Full Text] [Related]
18. Terminal deletion of the long arm of chromosome 10 : q26 to qter. Case report and review of literature.
Taysi K; Strauss AW; Yang V; Padmalatha C; Marshall RE
Ann Genet; 1982; 25(3):141-4. PubMed ID: 6982660
[TBL] [Abstract][Full Text] [Related]
19. Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies.
Back E; Hertel C; Vogel W; Bettecken F; Thiesen M
Ann Genet; 1977 Dec; 20(4):294-6. PubMed ID: 305761
[TBL] [Abstract][Full Text] [Related]
20. A clinical syndrome associated with 5p duplication and 9p deletion.
Liberfarb RM; Atkins L; Holmes LB
Ann Genet; 1980; 23(1):26-30. PubMed ID: 6965836
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
