298 related articles for article (PubMed ID: 7395903)
1. Deletion of a portion of the long arm of chromosome 6.
Goldberg R; Fish B; Ship A; Shprintzen RJ
Am J Med Genet; 1980; 5(1):73-80. PubMed ID: 7395903
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
Zenger-Hain JL; Roberson J; Van Dyke DL; Weiss L
Am J Med Genet; 1993 Jun; 46(4):438-40. PubMed ID: 7689299
[TBL] [Abstract][Full Text] [Related]
3. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW
Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
[TBL] [Abstract][Full Text] [Related]
4. The syndrome of ring chromosome 12.
Scribanu N; McCullars EB; Baumiller RC; Colon AR
Am J Med Genet; 1980; 5(2):165-70. PubMed ID: 7395909
[TBL] [Abstract][Full Text] [Related]
5. Terminal deletion of the long arm of chromosome 4. Report of a case of 46, XY, del(4)(q31) and review of 4q- syndrome.
Yu CW; Chen H; Baucum RW; Hand AM
Ann Genet; 1981; 24(3):158-61. PubMed ID: 6974525
[TBL] [Abstract][Full Text] [Related]
6. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
Meng J; Fujita H; Nagahara N; Kashiwai A; Yoshioka Y; Funato M
Am J Med Genet; 1992 Jul; 43(4):747-50. PubMed ID: 1621768
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Deletions of the long arm of chromosome 6: two new cases and review of the literature.
Young RS; Fidone GS; Reider-Garcia PA; Hansen KL; McCombs JL; Moore CM
Am J Med Genet; 1985 Jan; 20(1):21-9. PubMed ID: 3881954
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Trisomy 22: no longer an enigma.
Kukolich MK; Kulharya A; Jalal SM; Drummond-Borg M
Am J Med Genet; 1989 Dec; 34(4):541-4. PubMed ID: 2624265
[TBL] [Abstract][Full Text] [Related]
11. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
Stratton RF; Dobyns WB; Greenberg F; DeSana JB; Moore C; Fidone G; Runge GH; Feldman P; Sekhon GS; Pauli RM
Am J Med Genet; 1986 Jul; 24(3):421-32. PubMed ID: 3728561
[TBL] [Abstract][Full Text] [Related]
12. Malformation syndrome of duplication 12q24.1 leads to qter.
Melnyk AR; Weiss L; Van Dyke DL; Jarvi P
Am J Med Genet; 1981; 10(4):357-65. PubMed ID: 7332029
[TBL] [Abstract][Full Text] [Related]
13. A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2.
Ramer JC; Ladda RL; Frankel CA; Beckford A
Am J Med Genet; 1989 Mar; 32(3):359-63. PubMed ID: 2658585
[TBL] [Abstract][Full Text] [Related]
14. [Ring chromosome 13 and multiple malformations (author's transl)].
Antich J; Plaza J; Geán E
An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.
Dobyns WB; Dewald GW; Carlson RO; Mair DD; Michels VV
Am J Med Genet; 1985 Sep; 22(1):125-34. PubMed ID: 3901750
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Partial duplication of distal 17q.
Bridge J; Sanger W; Mosher G; Buehler B; Hearty C; Olney A; Fordyce R
Am J Med Genet; 1985 Oct; 22(2):229-35. PubMed ID: 4050855
[TBL] [Abstract][Full Text] [Related]
19. Deletion of the distal long arm of chromosome 1: a definable syndrome.
Johnson VP; Heck LJ; Carter GA; Flom JO
Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121
[TBL] [Abstract][Full Text] [Related]
20. Constitutional del(5)(q23.3q31.1).
Rivera H; Garcia-Esquivel L; Moller M; Cantú JM
Ann Genet; 1987; 30(2):91-3. PubMed ID: 3499848
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]