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23. Cytogenetic abnormalities in orthopedic patients. Cowell HR; Clark CE Clin Orthop Relat Res; 1978 Sep; (135):4-14. PubMed ID: 152176 [TBL] [Abstract][Full Text] [Related]
24. Fragile X-chromosome among child psychiatric patients with disturbances of language and social relationships. A pilot study. Jørgensen OS; Nielsen KB; Isager T; Mouridsen SE Acta Psychiatr Scand; 1984 Nov; 70(5):510-4. PubMed ID: 6516896 [TBL] [Abstract][Full Text] [Related]
25. Multiple chromosome aberrations: XO-XY-XYY mosaicism and a translocation in the same family. Ferrier PE; Ferrier SA; Schärer KO; Genton N; Hedinger C; Klein D Helv Paediatr Acta; 1967 Dec; 22(6):516-28. PubMed ID: 5592961 [No Abstract] [Full Text] [Related]
27. Which chromosomal syndromes can be managed medically. de Grouchy J Prog Clin Biol Res; 1979; 34():81-96. PubMed ID: 161024 [No Abstract] [Full Text] [Related]
28. [Indications for chromosome analysis]. Pfeiffer RA Fortschr Med; 1985 Jan; 103(3):33-6. PubMed ID: 3156080 [No Abstract] [Full Text] [Related]
29. Heterotopic-bone formation in two males with the 47,XYY karyotype. Price WH; Fraser GM Lancet; 1969 Nov; 2(7630):1134. PubMed ID: 4188072 [No Abstract] [Full Text] [Related]
30. [Distal deletion at 11q and language delay]. Pérez Castillo A; Mardomingo Sanz MJ; Abrisqueta Zarrabe JA An Esp Pediatr; 1989 Mar; 30(3):242-4. PubMed ID: 2729803 [TBL] [Abstract][Full Text] [Related]
31. Developmental trends of communicative skills in children with chromosome 14 aberrations. Zampini L; Zanchi P; Rinaldi B; Novara F; Zuffardi O Eur J Pediatr; 2017 Apr; 176(4):455-464. PubMed ID: 28124115 [TBL] [Abstract][Full Text] [Related]
32. [Gonosomal trisomy syndrome. Five case reports and review of literature]. Schwemmle C; Jungheim M; Ptok M Laryngorhinootologie; 2013 Nov; 92(11):725-31. PubMed ID: 23929211 [TBL] [Abstract][Full Text] [Related]
33. Deletion - translocation del (12) (p11) leads to (t10;12) (p13;pII). Nielsen J; Rasmussen K; Niebuhr E Ann Genet; 1976 Mar; 19(1):53-5. PubMed ID: 1084123 [TBL] [Abstract][Full Text] [Related]
34. Developmental dyspraxia in a family with X-linked mental retardation (Renpenning syndrome). McLaughlin JF; Kriegsmann E Dev Med Child Neurol; 1980 Feb; 22(1):84-92. PubMed ID: 7188916 [TBL] [Abstract][Full Text] [Related]
35. [Speech disorders in children of aphasic fathers- a developmental psycholinguistic case study]. Mattejat F; Niebergall G; Nestler V Prax Kinderpsychol Kinderpsychiatr; 1980 Apr; 29(3):83-9. PubMed ID: 7393866 [No Abstract] [Full Text] [Related]
36. On the deletion 4p16 Wolf-Hirschhorn syndrome. Rivas F; Hernandez A; Nazara Z; Fragoso R; Olivares N; Rolon A; Cantu JM Ann Genet; 1979; 22(4):228-31. PubMed ID: 317787 [TBL] [Abstract][Full Text] [Related]
37. 18q- and 18q+ mosaicism in a mentally retarded boy. Ausems MG; Bhola SL; Post-Blok CA; Hennekam RC; de France HF Am J Med Genet; 1994 Nov; 53(3):296-9. PubMed ID: 7856666 [TBL] [Abstract][Full Text] [Related]
38. [The chromosomal syndromes (author's transl)]. Klein D Padiatr Padol Suppl; 1975; 4():1-31. PubMed ID: 127145 [TBL] [Abstract][Full Text] [Related]
39. Oligohydramnios syndrome and XYY karyotype. Côté GB; Tsomi K; Papadakou-Lagoyanni S; Petmezaki S Ann Genet; 1978 Dec; 21(4):226-8. PubMed ID: 314260 [TBL] [Abstract][Full Text] [Related]
40. Chromosomal studies in relation to abortion. Adler P; Gierke LW J Am Osteopath Assoc; 1971 Aug; 70(12):1319-23. PubMed ID: 4255173 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]