270 related articles for article (PubMed ID: 3477100)
1. Deletion of 2p: a cytogenetic and clinical update.
Neidich J; Zackai E; Aronson M; Emanuel BS
Am J Med Genet; 1987 Jul; 27(3):707-10. PubMed ID: 3477100
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion of chromosome 2 (p23p25).
Penchaszadeh VB; Dowling PK; Davis JG; Schmidt R; Wapnir RA
Am J Med Genet; 1987 Jul; 27(3):701-6. PubMed ID: 3477099
[TBL] [Abstract][Full Text] [Related]
3. Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2.
Saal HM; King LJ; Zimmerman D; Johnson RC; Carr AG; Samango-Sprouse CA; Stanley W
Am J Med Genet; 1996 Dec; 66(4):373-7. PubMed ID: 8989454
[TBL] [Abstract][Full Text] [Related]
4. Deletion mapping: further evidence for the location of acid phosphatase (ACP1) within 2p23.
Emanuel BS; Zackai EH; Van Dyke DC; Swallow DM; Allen FH; Mellman WJ
Am J Med Genet; 1979; 4(2):167-72. PubMed ID: 293131
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
Taysi K; Dengler DR; Jones LA; Heersma JR
Ann Genet; 1981; 24(4):245-7. PubMed ID: 7036843
[No Abstract] [Full Text] [Related]
6. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
Fryns JP; Kleczkowska A; Kenis H; Decock P; Van den Berghe H
Ann Genet; 1989; 32(3):174-6. PubMed ID: 2573314
[TBL] [Abstract][Full Text] [Related]
7. Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5.
Keppen LD; Gollin SM; Edwards D; Sawyer J; Wilson W; Overhauser J
Am J Med Genet; 1992 Oct; 44(3):356-60. PubMed ID: 1488985
[TBL] [Abstract][Full Text] [Related]
8. Distal monosomy of the long arm of chromosome 6 (6q25----6qter) inherited by maternal translocation t(6q;17q).
Oliveira-Duarte MH; Martelli-Soares LR; Sarquis-Cintra T; Machado ML; Lison MP
Ann Genet; 1990; 33(1):56-9. PubMed ID: 2195984
[TBL] [Abstract][Full Text] [Related]
9. Isochromosome-formation in chromosome 9.
Miller K; Arslan-Kirchner M
Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983
[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. 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]
12. Normal phenotype and slight mental retardation in de novo distal 8p deletion (8pter----8p23.1:).
Fryns JP; Kleczkowska A; Vogels A; Van den Berghe H
Ann Genet; 1989; 32(3):171-3. PubMed ID: 2573313
[TBL] [Abstract][Full Text] [Related]
13. Interstitial deletion of (17)(p11.2). A microdeletion syndrome. Another example.
de Almeida JC; Reis DF; Martins RR
Ann Genet; 1989; 32(3):184-6. PubMed ID: 2817780
[TBL] [Abstract][Full Text] [Related]
14. [Wolf syndrome. Apropos of 2 cases].
García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
[TBL] [Abstract][Full Text] [Related]
15. Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2.
McMilin KD; Reiss JA; Brown MG; Black MH; Buckmaster DA; Durum CT; Gunter KA; Lawce HJ; Berry TL; Lamb OA; Olson CL; Weeks FF; Yoshitomi MJ; Jacky PB; Olson SB; Magenis RE
Am J Med Genet; 1998 Jun; 78(1):36-43. PubMed ID: 9637421
[TBL] [Abstract][Full Text] [Related]
16. Choanal atresia in a patient with the deletion (9p) syndrome.
Shashi V; Golden WL; Fryburg JS
Am J Med Genet; 1994 Jan; 49(1):88-90. PubMed ID: 8172257
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Neuroblastoma in patients with constitutional chromosomal changes.
Fryns JP
Genet Couns; 1996; 7(1):73. PubMed ID: 8652093
[No Abstract] [Full Text] [Related]
19. Clinical and molecular analyses of deletion 3p25-pter syndrome.
Mowrey PN; Chorney MJ; Venditti CP; Latif F; Modi WS; Lerman MI; Zbar B; Robins DB; Rogan PK; Ladda RL
Am J Med Genet; 1993 Jul; 46(6):623-9. PubMed ID: 8103286
[TBL] [Abstract][Full Text] [Related]
20. Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome.
Clementi M; Tenconi R; Turolla L; Silvan C; Bortotto L; Artifoni L
Am J Med Genet; 1991 Nov; 41(2):246-50. PubMed ID: 1785643
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
