106 related articles for article (PubMed ID: 1920913)
1. De novo interstitial deletion of 4q[46,XX,del(4)(q27q28.2)] with intact blood group-MN locus, confining its locus to 4q28.2-4q31.1.
Wakui K; Nishida T; Masuda J; Itoh T; Katsumata D; Ohno T; Fukushima Y
Jinrui Idengaku Zasshi; 1991 Jun; 36(2):149-53. PubMed ID: 1920913
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion of chromosome 2 region in a malformed infant.
Melnyk AR; Muraskas J
Am J Med Genet; 1993 Jan; 45(1):49-51. PubMed ID: 8418659
[TBL] [Abstract][Full Text] [Related]
3. Interstitial deletion of 4(q21q25) in a liveborn male.
Rose NC; Schneider A; McDonald-McGinn DM; Caserta C; Emanuel BS; Zackai EH
Am J Med Genet; 1991 Jul; 40(1):77-9. PubMed ID: 1887853
[TBL] [Abstract][Full Text] [Related]
4. Interstitial 7q deletion [46,XX,del(7)(pter----q21.1::q22----qter)] and the location of genes for beta-glucuronidase and cystic fibrosis.
Chitayat D; McGillivray BC; Wood S; Kalousek DK; Langlois S; Applegarth DA
Am J Med Genet; 1988 Nov; 31(3):655-61. PubMed ID: 3228144
[TBL] [Abstract][Full Text] [Related]
5. [De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child].
Turleau C; Roubin M; Chavin-Colin F; Satge M; de Grouchy J
Ann Genet; 1974 Dec; 17(4):291-4. PubMed ID: 4548828
[No Abstract] [Full Text] [Related]
6. 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]
7. Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].
Chitayat D; Babul R; Silver MM; Jay V; Teshima IE; Babyn P; Becker LE
Am J Med Genet; 1996 Jan; 61(1):45-8. PubMed ID: 8741917
[TBL] [Abstract][Full Text] [Related]
8. The 4q-Syndrome.
Strehle EM; Ahmed OA; Hameed M; Russell A
Genet Couns; 2001; 12(4):327-39. PubMed ID: 11837601
[TBL] [Abstract][Full Text] [Related]
9. A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum.
Genuardi M; Calvieri F; Tozzi C; Coslovi R; Neri G
Clin Dysmorphol; 1994 Oct; 3(4):292-6. PubMed ID: 7894733
[TBL] [Abstract][Full Text] [Related]
10. Interstitial deletion of the long arm of chromosome 2 in a malformed infant with karyotype 46,XX,del(2)(q31q33).
Benson K; Gordon M; Wassman ER; Tsi C
Am J Med Genet; 1986 Nov; 25(3):405-11. PubMed ID: 3789004
[TBL] [Abstract][Full Text] [Related]
11. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.
Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS
Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241
[TBL] [Abstract][Full Text] [Related]
12. [Del(1)(q22-q25) syndrome. Cytogenetics and phenotype].
Zaletaev DV; Dadali EL; Kuleshov NP
Tsitol Genet; 1987; 21(3):213-6. PubMed ID: 3617217
[TBL] [Abstract][Full Text] [Related]
13. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
[TBL] [Abstract][Full Text] [Related]
14. Terminal deletion 4q in a severely retarded boy.
de Michelena MI; Campos PJ
Am J Med Genet; 1989 Jun; 33(2):228-30. PubMed ID: 2764033
[TBL] [Abstract][Full Text] [Related]
15. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
Lin AE; Garver KL; Diggans G; Clemens M; Wenger SL; Steele MW; Jones MC; Israel J
Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
[TBL] [Abstract][Full Text] [Related]
16. Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.
Kulharya AS; Maberry M; Kukolich MK; Day DW; Schneider NR; Wilson GN; Tonk V
Am J Med Genet; 1995 Jan; 55(2):165-70. PubMed ID: 7717415
[TBL] [Abstract][Full Text] [Related]
17. Two patients with interstitial del (14q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-1-antitrypsin).
Turleau C; de Grouchy J; Chavin-Colin F; Dore F; Seger J; Dautzenberg MD; Arthuis M; Jeanson C
Ann Genet; 1984; 27(4):237-40. PubMed ID: 6335371
[TBL] [Abstract][Full Text] [Related]
18. Centric fission of chromosome 7 with 47,XX,del(7)(pter----cen::q21----qter)+cen fr karyotype in a mother and proximal 7q deletion in two malformed newborns.
Fryns JP; Kleczkowska A; Limbos C; Vandecasseye W; Van den Berghe H
Ann Genet; 1985; 28(4):248-50. PubMed ID: 3879440
[TBL] [Abstract][Full Text] [Related]
19. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
[TBL] [Abstract][Full Text] [Related]
20. Interstitial deletion of the distal long arm of chromosome 4.
Sarda P; Lefort G; Fryns JP; Humeau C; Rieu D
J Med Genet; 1992 Apr; 29(4):259-61. PubMed ID: 1583648
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
