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2. "Pure" monosomy 21 pter leads to q21 in a girl born to a couple 46,XX,t(14;21)(p12;q22) and 46,XY,t(5;18)(q32;q22). Rivera H; Rivas F; Plascencia L; Cantú JM Ann Genet; 1983; 26(4):234-7. PubMed ID: 6607704 [TBL] [Abstract][Full Text] [Related]
3. [Partial trisomy 13 for the distal long arm and its prenatal diagnosis]. Zolotukhina TV; Rozovskiĭ IS; Bartseva OB; Vakhlamova IV; Bubnova NI Genetika; 1982 Nov; 18(11):1899-905. PubMed ID: 6891355 [TBL] [Abstract][Full Text] [Related]
5. [Ring chromosome 13 and multiple malformations (author's transl)]. Antich J; Plaza J; Geán E An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149 [TBL] [Abstract][Full Text] [Related]
6. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy". Curry CJ; Ying KL; O'Lague P; Tsai J Birth Defects Orig Artic Ser; 1982; 18(3B):275-86. PubMed ID: 7139110 [No Abstract] [Full Text] [Related]
7. De novo tandem duplication of the middle segment of the long arm of chromosome 14. Ito M; Mutoh K; Okuno T; Mikawa H; Edagawa J; Abe T Ann Genet; 1983; 26(2):116-9. PubMed ID: 6604486 [TBL] [Abstract][Full Text] [Related]
8. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15. Cohen MM; Ornoy A; Rosenmann A; Kohn G Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372 [TBL] [Abstract][Full Text] [Related]
9. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)]. Butomo IV; Prozorova MV; Khitrikova LE Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655 [TBL] [Abstract][Full Text] [Related]
10. Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families. Prieto F; Badia L; Asensi F; Roques V Hum Genet; 1980; 54(1):7-11. PubMed ID: 7390483 [TBL] [Abstract][Full Text] [Related]
11. Distal trisomy 14q due to tandem duplication (q24 leads to q32). Orye E; Van Bever H; Desimpel H Ann Genet; 1983; 26(4):238-9. PubMed ID: 6607705 [TBL] [Abstract][Full Text] [Related]
12. [Balanced translocations with abnormal phenotype (author's transl)]. Taillemite JL; Portnoi MF; Van den Akker J; Leporrier N; Marmor D; Roux C J Gynecol Obstet Biol Reprod (Paris); 1978 Apr; 7(3):407-17. PubMed ID: 681696 [TBL] [Abstract][Full Text] [Related]
13. 8q22-->qter duplication in a child with multiple congenital malformations: case report. Sasiadek M; Stembalska A; Schlade K; Zych M Med Sci Monit; 2000; 6(1):141-4. PubMed ID: 11208302 [TBL] [Abstract][Full Text] [Related]
14. [Interstitial deletion of the long arms of chromosome 13]. Molina M; Santolaya JM; Onaindía ML; Sánchez E; De Gárate J An Esp Pediatr; 1982 Apr; 16(4):346-51. PubMed ID: 7125394 [TBL] [Abstract][Full Text] [Related]
15. Duplication 11 (q22----qter) in an infant. A case report with review. Greig F; Rosenfeld W; Verma RS; Babu KA; David K Ann Genet; 1985; 28(3):185-8. PubMed ID: 3879155 [TBL] [Abstract][Full Text] [Related]
16. Inherited chromosomal translocation in two families (t(4q-;13q+) and t(5q-; 13q+)). Watanabe G; Kiyoi Y; Takeyama I; Kawana S; Yamamoto M Tohoku J Exp Med; 1977 Feb; 121(2):179-84. PubMed ID: 847744 [TBL] [Abstract][Full Text] [Related]