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.
6. [Genetics of neuropsychiatric disorders]. Cacabelos R Med Clin (Barc); 1990 May; 94(18):699-701. PubMed ID: 2388495 [No Abstract] [Full Text] [Related]
7. Duplication (12p) syndrome--a family. O'Sullivan BJ; Murphy A; Asghar M Ir Med J; 1995; 88(3):106. PubMed ID: 7635680 [TBL] [Abstract][Full Text] [Related]
8. Behavioral phenotypes of genetic syndromes: a reference guide for psychiatrists. Moldavsky M; Lev D; Lerman-Sagie T J Am Acad Child Adolesc Psychiatry; 2001 Jul; 40(7):749-61. PubMed ID: 11437013 [TBL] [Abstract][Full Text] [Related]
9. [136 karyotypes in psychiatry: surprising results]. Pascalis G; Bajolle F; Delpech J; Teyssier JR Ann Med Psychol (Paris); 1980 Mar; 138(3):304-10. PubMed ID: 7224483 [TBL] [Abstract][Full Text] [Related]
10. [Examination of fluorescence of Y chromosome in blood smears in mentally ill patients]. Oleĭnikov NI Lab Delo; 1973; 5():306-7. PubMed ID: 4129163 [No Abstract] [Full Text] [Related]
11. A new family with a satellited Y. Shabtai F; Eilam N; Elian E; Halbrecht I Ann Genet; 1981; 24(4):223-5. PubMed ID: 6977302 [No Abstract] [Full Text] [Related]
12. [Sex chromatin corpuscle in psychiatry]. Gini R; Caldararo JC; Pérez Arancibia L Prensa Med Argent; 1970 Mar; 57(2):64-7. PubMed ID: 5453138 [No Abstract] [Full Text] [Related]
13. A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes. Matheisel A; Babinska M; Wierzba J; Wozniak A; Nedoszytko B; Balcerska A; Limon J Genet Couns; 2000; 11(3):267-71. PubMed ID: 11043435 [TBL] [Abstract][Full Text] [Related]
14. [Incidence of psychopathological changes in adolescence with a large genetic component]. Salvanés Pérez R An Esp Pediatr; 1983 Sep; 19 Suppl 19():108-12. PubMed ID: 6660663 [No Abstract] [Full Text] [Related]
15. [Chromosomal syndromes in the autosomal system and the problems of differential diagnosis]. Grechanina EIa; Pesochina EA; Babadzhanian EN; Bondarenko AV Tsitol Genet; 1993; 27(4):61-6. PubMed ID: 8249166 [TBL] [Abstract][Full Text] [Related]
16. Trisomy 18-Edwards syndrome: a report of three patients. Ejiwumni AB; Msamati BC Cent Afr J Med; 1993 May; 39(5):105-9. PubMed ID: 8131193 [No Abstract] [Full Text] [Related]
17. Form of 15q proximal duplication appears to be a normal euchromatic variant. Jalal SM; Persons DL; Dewald GW; Lindor NM Am J Med Genet; 1994 Oct; 52(4):495-7. PubMed ID: 7747767 [No Abstract] [Full Text] [Related]
18. Identifying sex chromosome abnormalities in forensic DNA testing using amelogenin and sex chromosome short tandem repeats. Young DR; Tun Z; Honda K; Matoba R J Forensic Sci; 2001 Mar; 46(2):346-8. PubMed ID: 11305438 [TBL] [Abstract][Full Text] [Related]
19. Holt-Oram syndrome with associated postaxial and central polydactyly. Further evidence for genetic heterogeneity in the Holt-Oram syndrome. Fryns JP; Bonnet D; De Smet L Genet Couns; 1996; 7(4):323-4. PubMed ID: 8985738 [No Abstract] [Full Text] [Related]
20. Ring chromosome 15 syndrome in an adult female. Matsuishi T; Yamada Y; Endo K; Sakai H; Fukushima Y J Intellect Disabil Res; 1996 Oct; 40 ( Pt 5)():478-80. PubMed ID: 8906535 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]