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3. Autosomal chromosome aberrations. A review of the clinical syndromes caused by structural chromosome aberrations, mosaic-trisomies 8 and 9, and triploidy. Schinzel A Ergeb Inn Med Kinderheilkd; 1976; 38():37-94. PubMed ID: 782877 [No Abstract] [Full Text] [Related]
4. Clinical, cytogenetic and autoradiographic studies in 10 cases with rare chromosome disorders II. Cases 3,4 and 5. Moore MK; Engel E Ann Genet; 1970 Jun; 13(2):129-34. PubMed ID: 5310697 [No Abstract] [Full Text] [Related]
5. Partial trisomy 9 in the case of familial translocation 8/9 mat. Schwanitz G; Schamberger U; Rott HD; Wieczorek V Ann Genet; 1974 Sep; 17(3):163-6. PubMed ID: 4548816 [No Abstract] [Full Text] [Related]
6. Partial trisomy of chromosome 11: a case report. Falk RE; Carrel RE; Valente M; Crandall BF; Sparkes RS Am J Ment Defic; 1973 Jan; 77(4):383-8. PubMed ID: 4706396 [No Abstract] [Full Text] [Related]
7. [Cp trisomy: a new syndrome]. Canu JM; Buentello L; Armendares S Ann Genet; 1971 Sep; 14(3):177-86. PubMed ID: 5315464 [No Abstract] [Full Text] [Related]
8. [The intelligence level in the chromosome aberrations affecting autosomes]. Moor L Rev Neuropsychiatr Infant; 1970 Dec; 18(12):943-66. PubMed ID: 4251821 [No Abstract] [Full Text] [Related]
9. ["Free" 9p trisomy in a male child with severe mental retardation (author's transl)]. Aller V; Abrisqueta JA; Martín-Lucas MA; de Torres ML; del Mazo J; Pérez-Castillo A An Esp Pediatr; 1979 May; 12(5):463-8. PubMed ID: 464416 [TBL] [Abstract][Full Text] [Related]
10. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies. Oikawa K; Kajii T; Shimba H; Sasaki M Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379 [No Abstract] [Full Text] [Related]
11. Structural aberrations of autosomes in a mentally retarded population. Corey MJ; Tischler B; Sandercock J Am J Ment Defic; 1971 Jan; 75(4):487-98. PubMed ID: 4251270 [No Abstract] [Full Text] [Related]
12. [Clinical anatomic and histopathological study of ocular signs in 2 cases of mosaicism associated with autosomal 18-21 double trisomy]. Laliam M; Laliam N; Ouadahi MS; Iles S; Ould Larbi L Bull Mem Soc Fr Ophtalmol; 1972; 85(0):83-90. PubMed ID: 4211332 [No Abstract] [Full Text] [Related]
13. [Trisomy of group C (47, XX, C+)]. Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R Arch Fr Pediatr; 1970; 27(10):1081-8. PubMed ID: 5495708 [No Abstract] [Full Text] [Related]
14. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity]. Rethoré MO; Larget-Piet L; Abonyi D; Boeswillwald M; Berger R; Carpentier S; Cruveiller J; Dutrillau B; Lafourcade J; Penneau M; Lejeune J Ann Genet; 1970 Dec; 13(4):217-32. PubMed ID: 5313386 [No Abstract] [Full Text] [Related]
16. [Monosomy 21 with mosaicism 45,XX,21--46,XX,21 pi]. Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R Arch Fr Pediatr; 1970; 27(10):1069-79. PubMed ID: 5495707 [No Abstract] [Full Text] [Related]
17. [Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+]. de Grouchy J; Turleau C; Léonard C Ann Genet; 1971 Mar; 14(1):69-72. PubMed ID: 5314298 [No Abstract] [Full Text] [Related]
18. [Clinical and cytogenetic observations on 2 mosaic C trisomic adults. Individualization of the supernumerary chromosome with the modern denaturation technic: 47, XY, ?8 +]. Laurent C; Robert JM; Grambert J; Dutrillaux B Lyon Med; 1971 Dec; 226(20):827-33. PubMed ID: 5144392 [No Abstract] [Full Text] [Related]
19. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat]. Di Cesare D; Paludetto R; Casullo C; Pagano L; Stabile M; Sicolo A; Ventruto V Minerva Pediatr; 1980 Dec; 32(23):1349-52. PubMed ID: 7219376 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]