These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
120 related articles for article (PubMed ID: 6711357)
1. [Trisomy 20p]. Zergollern L; Begović D Acta Med Iugosl; 1984; 38(1):69-75. PubMed ID: 6711357 [No Abstract] [Full Text] [Related]
2. Inverted tandem duplication of the middle segment of the long arm of chromosome 14. Strain JE; Smith AC; Ward BE; Robinson A Pediatrics; 1981 Feb; 67(2):273-6. PubMed ID: 7243453 [No Abstract] [Full Text] [Related]
3. "De Novo" trisomy 20p with macroorchidism in a prepuberal boy. Balestrazzi P; Virdis R; Frassi C; Negri V; Rigoli E; Bernasconi S Ann Genet; 1984; 27(1):58-9. PubMed ID: 6609676 [TBL] [Abstract][Full Text] [Related]
4. [Elfin face syndrome - an often missed diagnosis]. Zetterqvist P; Klackenberg G; Billing L; Bjarke B; Josephsson E; Lundström NR Lakartidningen; 1982 Apr; 79(14):1363-6. PubMed ID: 7087611 [No Abstract] [Full Text] [Related]
5. 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]
6. A syndrome of craniofacial, digital, and genital anomalies. Harrod MJ; Keele DK; Howard J Birth Defects Orig Artic Ser; 1977; 13(3B):111-5. PubMed ID: 890088 [No Abstract] [Full Text] [Related]
7. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development. Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090 [TBL] [Abstract][Full Text] [Related]
8. [Monosomy/trisomy 4q12 to q13 mosaicism in a retarded and dysmorphic girl]. Pescia G; Tonella A; Jotterand-Bellomo M Ann Genet; 1982; 25(2):110-2. PubMed ID: 6984625 [No Abstract] [Full Text] [Related]
9. Duplication 8q syndrome due to familial chromosome ins(10;8)(q21;q212q22). Bowen P; Fitzgerald PH; Gardner RJ; Biederman B; Veale AM Am J Med Genet; 1983 Apr; 14(4):635-46. PubMed ID: 6846399 [TBL] [Abstract][Full Text] [Related]
10. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features. Mégarbané A; Souraty N; Theophile D; Vekemans M; Samaras L; Ghorayeb Z Ann Genet; 1997; 40(1):55-9. PubMed ID: 9150851 [TBL] [Abstract][Full Text] [Related]
11. [Rubinstein-Taybi syndrome. A propos of 2 new cases]. Biscatti G; Cagini P; Brushchelli M Pediatria (Napoli); 1971 Dec; 79(4):491-501. PubMed ID: 5142979 [No Abstract] [Full Text] [Related]
12. [Juvenile cerebral spongiosis]. Tridon P; Martin JJ; Vidailhet M; Floquet J; Philippart M; Neimann N Pediatrie; 1974; 29(3):235-47. PubMed ID: 4140493 [No Abstract] [Full Text] [Related]
13. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype. D'Amato Sizonenko L; Ng D; Oei P; Winship I Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728 [TBL] [Abstract][Full Text] [Related]
14. [Kabuki syndrome in the differential diagnosis of neonatal hypotonia]. Aguilera Albesa S; Botella Astorqui MP; Ocio Ocio I An Pediatr (Barc); 2009 Jan; 70(1):91-3. PubMed ID: 19174128 [No Abstract] [Full Text] [Related]
15. [Trisomy of the chromosome 18 in a mentally retarded child with hyperphenylalaninemia]. Adámek R; Zahálková M; Podhradská O; Saxl O; Mrskos A Acta Paediatr Acad Sci Hung; 1972; 13(1):33-7. PubMed ID: 4652494 [No 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. Trisomy 20p from maternal t(3;20) translocation. Archidiacono N; Tecilazich D; Tonini G; Rocchi M; Filippi G J Med Genet; 1979 Jun; 16(3):229-32. PubMed ID: 469903 [TBL] [Abstract][Full Text] [Related]