292 related articles for article (PubMed ID: 3879155)
1. Duplication 11 (q22----qter) in an infant. A case report with review.
Greig F; Rosenfeld W; Verma RS; Babu KA; David K
Ann Genet; 1985; 28(3):185-8. PubMed ID: 3879155
[TBL] [Abstract][Full Text] [Related]
2. [Partial trisomy 11q;22q (author's transl)].
Benítez J; Ayuso C; García Aparicio J; Sáez E; Pérez Sotelo A; Bello MJ
An Esp Pediatr; 1981 Sep; 15(3):293-300. PubMed ID: 7332142
[No Abstract] [Full Text] [Related]
3. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
Frankova YE; Holenova H; Braulke I
Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
[TBL] [Abstract][Full Text] [Related]
4. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
Taysi K; Chao WT; Monaghan N; Monaco MP
Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954
[TBL] [Abstract][Full Text] [Related]
5. De novo tandem duplication of the middle segment of the long arm of chromosome 14.
Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T
Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486
[TBL] [Abstract][Full Text] [Related]
6. [2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families].
Aurias A; Turc C; Michiels Y; Sinet PM; Graveleau D; Lejeune J
Ann Genet; 1975 Sep; 18(3):185-8. PubMed ID: 1080981
[TBL] [Abstract][Full Text] [Related]
7. Translocation/duplication of 9p onto a duplicated 4q.
Rivera H; Figuera LE; Vasquez AI
Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
[TBL] [Abstract][Full Text] [Related]
8. Phenotypic and cytogenetic spectrum of 9p trisomy.
Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
[TBL] [Abstract][Full Text] [Related]
9. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.
Courtens W; Wauters J; Wojciechowski M; Reyniers E; Scheers S; van Luijk R; Rooms L; Kooy F; Wuyts W
Clin Dysmorphol; 2007 Oct; 16(4):231-9. PubMed ID: 17786114
[TBL] [Abstract][Full Text] [Related]
10. [11q distal trisomy due to a familial 11;18 translocation].
Menéndez I; Rivera H; Morales E; Juan J; Jiménez M
Bol Med Hosp Infant Mex; 1990 Nov; 47(11):792-4. PubMed ID: 2285470
[TBL] [Abstract][Full Text] [Related]
11. Cri du chat-syndrome in combination with partial trisomy 9 p.
Sigmund J; Frisch H; Heinz-Erian P; Rhomberg K; Wegner RD
Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564
[TBL] [Abstract][Full Text] [Related]
12. [Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].
Ayraud N; Galiana A; Llyod M; Deswarte M
Ann Genet; 1976 Mar; 19(1):65-8. PubMed ID: 1084126
[TBL] [Abstract][Full Text] [Related]
13. [9p trisomy syndrome. Two new cases (author's transl)].
Martín Sánchez A; Delicado A; Izquierdo M; Oliver A; López Pajares I; Gracia R; Peralta A
An Esp Pediatr; 1981 May; 14(5):344-51. PubMed ID: 7294523
[TBL] [Abstract][Full Text] [Related]
14. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM
Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157
[TBL] [Abstract][Full Text] [Related]
15. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.
Ottolina de Bracamonte N; Velazco JQ; Hammond Figueroa FG
Acta Cient Venez; 1982; 33(4):342-7. PubMed ID: 7186725
[No Abstract] [Full Text] [Related]
16. [Trisomy 5p: a report of 2 cases].
Alvarez-Coca J; García-Alix A; Delicado A; González M; Escribá R; López Pajares I; Morena V; Peralta A
An Esp Pediatr; 1985 Mar; 22(4):288-92. PubMed ID: 4003955
[TBL] [Abstract][Full Text] [Related]
17. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
[TBL] [Abstract][Full Text] [Related]
18. Molecular and cytogenetic characterization of 9p- abnormalities.
Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
[TBL] [Abstract][Full Text] [Related]
19. [Reciprocal syndromes caused by deficiency duplication resulting from maternal t(10;18)(p12;q22) translocation].
Rethoré MO; Prieur M; de Blois MC; Naffah J; Ravel A; Villain E; Lejeune J
Ann Genet; 1985; 28(3):149-53. PubMed ID: 3879147
[TBL] [Abstract][Full Text] [Related]
20. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]