288 related articles for article (PubMed ID: 6513939)
1. [Phenotype of trisomy 9].
Pfeiffer RA; Müller R
Monatsschr Kinderheilkd; 1984 Oct; 132(10):797-800. PubMed ID: 6513939
[TBL] [Abstract][Full Text] [Related]
2. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
Shapiro SD; Hansen KL; Littlefield CA
Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720
[TBL] [Abstract][Full Text] [Related]
3. [Partial trisomy C by t(Cq-; Dp+) translocation with a C(p- q+) remnant].
De Grouchy J; Thieffry S; Aicardi J; Chevrie JJ; Zucker G
Arch Fr Pediatr; 1967 Oct; 24(8):859-68. PubMed ID: 5584189
[No Abstract] [Full Text] [Related]
4. [Chromosomal studies in craniofacial abnormalities].
Ahrens K
HNO; 1967 Apr; 15(4):106-9. PubMed ID: 5592377
[No Abstract] [Full Text] [Related]
5. Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).
Cantu JM; Salamanca F; Buentello L; Carnevale A; Armendares S
Ann Genet; 1975 Mar; 18(1):5-11. PubMed ID: 1080038
[TBL] [Abstract][Full Text] [Related]
6. [Tetrasomy 9p].
Foerster W; Koch M; Hansen S
Monatsschr Kinderheilkd; 1985 Sep; 133(9):694-7. PubMed ID: 2865673
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 12q interstitial deletion with bilateral cleft lip and palate: case report and literature review.
Yamanishi T; Nishio J; Miya S; Okamoto N; Takahashi A; Toribe Y; Mukai T; Kobayashi C
Cleft Palate Craniofac J; 2008 May; 45(3):325-8. PubMed ID: 18452363
[TBL] [Abstract][Full Text] [Related]
9. The phenotypic and cytogenetic spectrum of partial trisomy 9.
Wilson GN; Raj A; Baker D
Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Monosomy and trisomy of 15q24-qter with cleft lip and palate.
Abe A; Hatano Y; Kurita K; Nakano M; Shimizu M; Yokoi T; Sugiyama N
Int J Oral Maxillofac Surg; 2008 May; 37(5):487-90. PubMed ID: 18262763
[TBL] [Abstract][Full Text] [Related]
12. "Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21).
de Almeida JC; Reis DF; Llerena JC; Pereira ET
Ann Genet; 1989; 32(3):181-3. PubMed ID: 2817779
[TBL] [Abstract][Full Text] [Related]
13. Report of a trisomy 8p infant with carrier father.
Funderburk SJ; Barrett CT; Klisak I
Ann Genet; 1978 Dec; 21(4):219-22. PubMed ID: 314258
[TBL] [Abstract][Full Text] [Related]
14. Cleft palate and multiple anomalies in one of two siblings with partial 13 trisomy.
Kaye CI; Booth CW; Meeker D; Nadler HL
Cleft Palate J; 1977 Jul; 14(3):244-8. PubMed ID: 267527
[TBL] [Abstract][Full Text] [Related]
15. Trisomy 22 confirmed by fluorescent in situ hybridization.
Stratton RF; DuPont BR; Mattern VL; Young RS; McCourt JW; Moore CM
Am J Med Genet; 1993 Apr; 46(1):109-12. PubMed ID: 8494030
[TBL] [Abstract][Full Text] [Related]
16. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
Plotner PL; Smith JL; Northrup H
Am J Med Genet; 2002 Jul; 111(1):71-5. PubMed ID: 12124739
[TBL] [Abstract][Full Text] [Related]
17. Dermatoglyphics in children suffering from congenital defects, with and without chromosomal aberrations.
Usoev SS
Sov Genet; 1974 Jul; 8(7):929-31. PubMed ID: 4278489
[No Abstract] [Full Text] [Related]
18. [Fluorescence and Giemsa-banding in a case of Pätau's syndrome].
Golob E; Schaller A
Zentralbl Gynakol; 1974 Oct; 96(41):1305-8. PubMed ID: 4142346
[No Abstract] [Full Text] [Related]
19. Mosaic trisomy 9 syndrome with unusual phenotype.
Kaminker CP; Daín L; Lamas MA; Sánchez JM
Am J Med Genet; 1985 Oct; 22(2):237-41. PubMed ID: 3931476
[TBL] [Abstract][Full Text] [Related]
20. Oral-facial-digital (OFD) syndrome with associated features: a new syndrome or genetic heterogeneity and variability?
Morán-Barroso V; Valdés Flores M; García-Cavazos R; Kofman-Alfaro S; Saavedra-Ontiveros D
Clin Dysmorphol; 1998 Jan; 7(1):55-7. PubMed ID: 9546832
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
