137 related articles for article (PubMed ID: 6873945)
1. Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation.
Franceschini P; Cirillo Silengo M; Davi G; Bianco R; Biagioli M
Hum Genet; 1983; 64(1):98. PubMed ID: 6873945
[No Abstract] [Full Text] [Related]
2. Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies.
Franceschini P; Cirillo Silengo M; Davi G; Bianco R; Biagioli M
Hum Genet; 1983; 64(1):97. PubMed ID: 6873944
[No Abstract] [Full Text] [Related]
3. Interstitial deletion of chromosome 1 (q23-q25). Report of a case.
Silengo MC; Davi GF; Bianco R; Biagioli M; Guala A; Franceschini P; Novelli G
Clin Genet; 1984 Jun; 25(6):549-52. PubMed ID: 6587954
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Interstitial deletion of the long arm of chromosome 2: del(2)(q31q33).
Al-Awadi SA; Farag TI; Naguib K; Teebi A; Cuschieri A; Al-Othman S; Sundareshan TS
J Med Genet; 1983 Dec; 20(6):464-5. PubMed ID: 6655673
[TBL] [Abstract][Full Text] [Related]
6. Interstitial deletion of the long arm of chromosome 2: a case report and review of the literature.
Takahashi Y; Narahara K; Kikkawa K; Wakita Y; Kimura S; Murakami M; Kasai R; Kimoto H
Jinrui Idengaku Zasshi; 1985 Dec; 30(4):297-305. PubMed ID: 3869838
[No Abstract] [Full Text] [Related]
7. 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]
8. Terminal long-arm deletion of chromosome 1 in a male infant.
Dignan PS; Soukup S
Hum Genet; 1979 Apr; 48(2):151-6. PubMed ID: 457139
[TBL] [Abstract][Full Text] [Related]
9. Deletion of the short arm of chromosome 20.
Vianna-Morgante AM; Richieri-Costa A; Rosenberg C
Clin Genet; 1987 Jun; 31(6):406-9. PubMed ID: 3621644
[TBL] [Abstract][Full Text] [Related]
10. Terminal deletion with stable acentric fragment of 1q in a child with congenital malformations.
Kucerová M; Polívková Z; Dluholucký S; Kvasnicová M
Am J Hum Genet; 1983 Jan; 35(1):91-5. PubMed ID: 6823976
[TBL] [Abstract][Full Text] [Related]
11. De novo interstitial deletion del(1)(p21p32).
Bene M; Duca-Marinescu A; Ioan D; Maximilian C
J Med Genet; 1979 Aug; 16(4):323-7. PubMed ID: 490590
[TBL] [Abstract][Full Text] [Related]
12. Partial deletion of 1q, following a pericentric inversion, in a boy with multiple minor morphologic anomalies and mental retardation.
Schwanitz G; Schmid P; Hägele C; Daffner HW; Grosse KP
Acta Genet Med Gemellol (Roma); 1977; 26(2):173-5. PubMed ID: 596113
[TBL] [Abstract][Full Text] [Related]
13. Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation.
Silengo MC; Luzzatti L; Centerwall WR; Costello JM; Parslow M
Clin Genet; 1981 Mar; 19(3):174-80. PubMed ID: 7273460
[TBL] [Abstract][Full Text] [Related]
14. De novo direct tandem duplication of the proximal long arm of chromosome 2: 46,XX,dir dup(2)(q11 X 2q14 X 2).
Mu Y; Van Dyke DL; Weiss L; Olgac S
J Med Genet; 1984 Feb; 21(1):57-8. PubMed ID: 6694186
[TBL] [Abstract][Full Text] [Related]
15. A familial interstitial deletion of the long arm of chromosome 21.
Roland B; Cox DM; Hoar DI; Fowlow SB; Robertson AS
Clin Genet; 1990 Jun; 37(6):423-8. PubMed ID: 2383928
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Familial translocation t(3;22) detected in a carrier child with mental retardation and other abnormalities].
Gregori Romero M; Gil Benso R; López Ginés C; Pellín Pérez A; Barberá Guillem E
An Esp Pediatr; 1984 Oct; 21(6):593-6. PubMed ID: 6524770
[TBL] [Abstract][Full Text] [Related]
18. Cat-like cry and mental retardation owing to 7q interstitial deletion (7q22 leads to 7q32).
Abuelo DN; Padre-Mendoza T
J Med Genet; 1982 Dec; 19(6):473-6. PubMed ID: 7154049
[TBL] [Abstract][Full Text] [Related]
19. Interstitial deletion of the long arm of chromosome 3.
Martsolf JT; Ray M
Ann Genet; 1983; 26(2):98-9. PubMed ID: 6604494
[TBL] [Abstract][Full Text] [Related]
20. Monosomy 1pter.
Yunis E; Quintero L; Leibovici M
Hum Genet; 1981; 56(3):279-82. PubMed ID: 7239511
[No Abstract] [Full Text] [Related]
[Next] [New Search]
