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2. [Mental retardation in the crying cat syndrome. Comparison of the intellectual level in the partial deletion of the short arm of chromosome 5 with trisomy 21 and deletions of chromosome 18. Apropos of 118 cases taken from the literature]. Moor L Rev Neuropsychiatr Infant; 1968 Mar; 16(3):257-67. PubMed ID: 5683042 [No Abstract] [Full Text] [Related]
3. Partial trisomy of chromosome 3(p14----p22) due to maternal insertional translocation. Kleczkowska A; Fryns JP; Van den Berghe H Ann Genet; 1984; 27(3):180-3. PubMed ID: 6334484 [No Abstract] [Full Text] [Related]
8. Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients. Utine GE; Celik T; Alanay Y; Alikaşifoğlu M; Boduroğlu K; Tunçbilek E; Aktaş D Turk J Pediatr; 2009; 51(3):199-206. PubMed ID: 19817261 [TBL] [Abstract][Full Text] [Related]
9. [A new observation of trisomy 11q due to t(11,22)(q23.1; q11.1) mat (author's transl)]. Chauveau P; Gruchy D; Herouin C; Levesque L Ann Genet; 1980; 23(4):213-5. PubMed ID: 6971598 [TBL] [Abstract][Full Text] [Related]
11. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation]. Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734 [No Abstract] [Full Text] [Related]
12. 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]
13. [Trisomy 20p]. Zergollern L; Begović D Acta Med Iugosl; 1984; 38(1):69-75. PubMed ID: 6711357 [No Abstract] [Full Text] [Related]
14. A case of nondisjunction of chromosome 21 (47,X,Yqs,+21) in an Indian family with Yqs. Reddy KS; Thomas IM; Narayanan HS Ann Genet; 1984; 27(3):194-6. PubMed ID: 6334487 [TBL] [Abstract][Full Text] [Related]
15. [Cytogenetic findings in chromosome mosaicism with clinical manifestations]. Dreiss M Med Welt; 1981 Dec; 32(51-52):1949-52. PubMed ID: 7329232 [No Abstract] [Full Text] [Related]
16. 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]
17. De novo trisomy 22 due to an extra 22Q-chromosome. Stoll C; Medeiros P; Pécheur H; Schnebelen A Ann Genet; 1997; 40(4):217-21. PubMed ID: 9526616 [TBL] [Abstract][Full Text] [Related]
18. [Trisomy 4p. Mirror duplication of the short arm of chromosome 4 de novo]. Boyer JP; Andrieux L; Noel L; Mottet J Neuropsychiatr Enfance Adolesc; 1983 Jul; 31(7):319-21. PubMed ID: 6621831 [No Abstract] [Full Text] [Related]
19. [Partial chromosomal aberrations. Considerations on a case of trisomy 21 caused by rob translocation (14; 21)]. Infortuna M; Barberio G; Monego A; Gattarello A Minerva Pediatr; 1983 Oct; 35(20):995-1000. PubMed ID: 6669158 [No Abstract] [Full Text] [Related]
20. Partial trisomy 1q and monosomy 18q due to a de novo t(1;18)(q25;q23). Solé MT; Rivera H; Sánchez-Corona J; Plascencia L; Cantú JM Ann Genet; 1983; 26(2):120-2. PubMed ID: 6604487 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]