126 related articles for article (PubMed ID: 9880219)
1. Fetus with Casamassima-Morton-Nance syndrome and an inherited (6;9) balanced translocation.
Daïkha-Dahmane F; Huten Y; Morvan J; Szpiro-Tapia S; Nessmann C; Eydoux P
Am J Med Genet; 1998 Dec; 80(5):514-7. PubMed ID: 9880219
[TBL] [Abstract][Full Text] [Related]
2. Fetus with Casamassima-Morton-Nance Syndrome and Limb-Body Wall Defect: Presentation of a Novel Association and Review of the Phenotype.
Salinas-Torres VM
Pediatr Dev Pathol; 2016; 19(2):159-64. PubMed ID: 26367183
[TBL] [Abstract][Full Text] [Related]
3. Spondylocostal dysostosis, anal and genitourinary malformations in a fetal case: a new case of Casamassima-Morton-Nance syndrome?
Thauvin-Robinet C; Laurent N; Rousseau T; Couvreur S; Cusin V; Callier P; Mugneret F; Durand C; Huet F; Sagot P; Faivre L
Eur J Med Genet; 2007; 50(1):85-91. PubMed ID: 17056308
[TBL] [Abstract][Full Text] [Related]
4. A fetus diagnosed with Casamassima-Morton-Nance syndrome with de novo del(8)(p23.1).
Sasaki A; Hayashi S; Oi R; Anami A; Hanaoka M; Miyazaki O; Matsuoka K; Sago H
Prenat Diagn; 2011 Apr; 31(4):407-9. PubMed ID: 21413036
[No Abstract] [Full Text] [Related]
5. 24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism.
Chen CP; Wang TH; Lin SP; Chern SR; Chen MR; Lee CC; Chen YJ; Wang W
Eur J Med Genet; 2006; 49(6):516-9. PubMed ID: 16769261
[TBL] [Abstract][Full Text] [Related]
6. Prenatal clinical characteristics of Casamassima-Morton-Nance syndrome.
Aguinaga M; Yllescas E; Canseco M; Machuca A; Acevedo S; Mayén Molina DG
Prenat Diagn; 2009 Feb; 29(2):175-6. PubMed ID: 19090487
[No Abstract] [Full Text] [Related]
7. Molecular analysis of a translocation (6;11)(p21;q25) in a girl with Jacobsen syndrome.
Aalfs CM; Hoovers JM; Wijburg FA
Am J Med Genet; 1999 Oct; 86(4):398-400. PubMed ID: 10494099
[No Abstract] [Full Text] [Related]
8. Townes-Brocks syndrome.
Powell CM; Michaelis RC
J Med Genet; 1999 Feb; 36(2):89-93. PubMed ID: 10051003
[TBL] [Abstract][Full Text] [Related]
9. [9p-syndrome].
Fujita H
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):318-9. PubMed ID: 11057244
[No Abstract] [Full Text] [Related]
10. Penoscrotal inversion, hypospadias, imperforate anus, facial anomalies, and developmental delay: definition of a new clinical syndrome.
Kuhnle U; Bartsch O; Werner W; Schuster T
Pediatr Surg Int; 2000; 16(5-6):396-9. PubMed ID: 10955572
[TBL] [Abstract][Full Text] [Related]
11. Townes-Brocks syndrome in an infant with translocation t (5;16).
Serville F; Lacombe D; Saura R; Billeaud C; Sergent MP
Genet Couns; 1993; 4(2):109-12. PubMed ID: 8357560
[TBL] [Abstract][Full Text] [Related]
12. Opitz trigonocephaly C syndrome in a boy with a de novo balanced reciprocal translocation t(3;18)(q13.13;q12.1).
Chinen Y; Kaname T; Yanagi K; Saito N; Naritomi K; Ohta T
Am J Med Genet A; 2006 Aug; 140(15):1655-7. PubMed ID: 16835930
[TBL] [Abstract][Full Text] [Related]
13. Partial trisomy 6q, due to balanced maternal translocation (6;22) (q21; p13) or (q21; pter).
Stamberg J; Shapiro J; Valle D; Kuhajda FP; Thomas G; Wissow L
Clin Genet; 1981 Feb; 19(2):122-5. PubMed ID: 7471508
[TBL] [Abstract][Full Text] [Related]
14. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
[TBL] [Abstract][Full Text] [Related]
15. "Understanding Adam" multiple reciprocal translocations: complex case presentation.
Linder CE; Lu X; Kim YM; Li S; Pineda J
J Perinat Neonatal Nurs; 2009; 23(2):150-6; quiz 157-8. PubMed ID: 19474586
[TBL] [Abstract][Full Text] [Related]
16. Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.
Tihy F; Lemyre E; Dallaire L; Lemieux N
Am J Med Genet; 2000 Apr; 91(5):383-6. PubMed ID: 10767003
[TBL] [Abstract][Full Text] [Related]
17. Characterization of a de novo balanced translocation t(9;18)(p23;q12.2) in a patient with oculoauriculovertebral spectrum.
Rooryck C; VuPhi Y; Souakri N; Burgelin I; Saura R; Lacombe D; Arveiler B; Taine L
Eur J Med Genet; 2010; 53(2):104-7. PubMed ID: 20132917
[TBL] [Abstract][Full Text] [Related]
18. Toriello-Carey syndrome and unbalanced translocation t(8;18)(p12;q22).
Martin-Denavit T; Till M; Plauchu H
Am J Med Genet A; 2004 Jul; 128A(2):219-21. PubMed ID: 15214022
[No Abstract] [Full Text] [Related]
19. CYCLOPIA AND OTHER DEFECTS IN A FETUS WITH UNIQUE CHROMOSOMAL REARRANGEMENT.
Golovataya EI; Pribushenya OV; Trebka EG; Novikova IV; Lurie IW
Genet Couns; 2015; 26(3):359-64. PubMed ID: 26625670
[No Abstract] [Full Text] [Related]
20. Complex translocation among chromosomes 2, 3, 9, 15, 18, 20 in a patient with 3p-syndrome.
Omrani MD; Saleh Gargari S; Azizi F; Safavi Naini N; Omrani S
Arch Iran Med; 2014 Jul; 17(7):521-2. PubMed ID: 24979567
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
