33 related articles for article (PubMed ID: 6869425)
1. [Translocation trisomy 4q in 2 siblings as a sequela of paternal balanced reciprocal translocation: t(1;4)(q44;q31)].
Bode H; Bühler EM; Wyler F; Hadzilselimovic F
Monatsschr Kinderheilkd; 1990 Nov; 138(11):763-6. PubMed ID: 2290435
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotype.
Quack B; Van Roy N; Verschraegen-Spae MR; Klein F
Ann Genet; 1992; 35(4):241-4. PubMed ID: 1296524
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
[TBL] [Abstract][Full Text] [Related]
4. Partial trisomy of chromosome 18 (pter leads to q11): a discussion on the identification of the critical segment.
San Martin V; Fernandez-Novoa C; Hevia A; Novales A; Fornell J; Galera H
Ann Genet; 1981; 24(4):248-50. PubMed ID: 6977308
[TBL] [Abstract][Full Text] [Related]
5. Trisomy 20p due to a paternal reciprocal translocation.
Funderburk SJ; Sparkes RS; Sparkes MC
Ann Genet; 1983; 26(2):94-7. PubMed ID: 6604493
[TBL] [Abstract][Full Text] [Related]
6. Language abnormalities and minimal physical anomalies in a boy with partial trisomy of chromosome 15.
Moedjono SJ; Needleman R; Funderburk SJ
Am J Ment Defic; 1983 May; 87(6):659-63. PubMed ID: 6869425
[No Abstract] [Full Text] [Related]
7. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
8. Familial 10p trisomy resulting from a maternal pericentric inversion.
Kozma C; Meck JM
Am J Med Genet; 1994 Feb; 49(3):281-7. PubMed ID: 8209887
[TBL] [Abstract][Full Text] [Related]
9. Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1q.
Lukusa T; Van Buggenhout G; Devriendt K; Meireleire J; Van Goethem G; Roelen L; Fryns JP
Ann Genet; 1998; 41(4):199-204. PubMed ID: 9881182
[TBL] [Abstract][Full Text] [Related]
10. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
van Buggenhout G; Decock P; Fryns JP
Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
[TBL] [Abstract][Full Text] [Related]
11. Duplication of (2)(q11.1-q13.2) in a boy with mental retardation and cleft lip and palate: another clefting gene locus on proximal 2q?
Riegel M; Schinzel A
Am J Med Genet; 2002 Jul; 111(1):76-80. PubMed ID: 12124740
[TBL] [Abstract][Full Text] [Related]
12. Mosaic isochromosome 8p.
Tilstra DJ; Grove M; Spencer AC; Norwood TH; Pagon RA
Am J Med Genet; 1993 Jun; 46(5):517-9. PubMed ID: 8322812
[TBL] [Abstract][Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]