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Journal Abstract Search
201 related items for PubMed ID: 3487277
1. Double autosomal chromosomal aberration (3p trisomy/9p monosomy) and sex-reversal. Fryns JP, Kleczkowska A, Casaer P, van den Berghe H. Ann Genet; 1986; 29(1):49-52. PubMed ID: 3487277 [Abstract] [Full Text] [Related]
2. Cri du chat-syndrome in combination with partial trisomy 9 p. Sigmund J, Frisch H, Heinz-Erian P, Rhomberg K, Wegner RD. Padiatr Padol; 1986; 21(1):61-7. PubMed ID: 3960564 [Abstract] [Full Text] [Related]
3. Partial trisomy 3p/monosomy 9p with sex reversal. Witters I, Vermeesch JR, Moerman PH, Fryns JP. Ultrasound Obstet Gynecol; 2004 Apr; 23(4):418-9. PubMed ID: 15065198 [No Abstract] [Full Text] [Related]
6. [Trisomy of the short arm of 9 with isochromosome 9p and partial monosomy Yq]. Geneix A, Jaffray JY, Charbonne F, Perissel B, Malpuech G, Malet P, Roland MO. Ann Genet; 1983 Apr; 26(2):103-5. PubMed ID: 6604482 [Abstract] [Full Text] [Related]
8. Clinicopathological study in a female infant with 46,XX,i(18q) showing mixed features of both trisomy 18 and monosomy 18p. Ieshima A, Takashima S, Takada K, Akamatsu Y, Ohtani K, Ando G. Jinrui Idengaku Zasshi; 1985 Sep; 30(3):219-26. PubMed ID: 3834202 [No Abstract] [Full Text] [Related]
10. Partial trisomy 6p and partial monosomy 9p from a de novo translocation 46,XY, -9, +DER(9)T(6:9)(p211:p24). Eden MS, Thelin JW, Michalski K, Mitchell JA. Clin Genet; 1985 Nov; 28(5):375-84. PubMed ID: 4085142 [Abstract] [Full Text] [Related]
11. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome. Lukusa T, van den Berghe L, Smeets E, Fryns JP. Ann Genet; 1999 Nov; 42(4):215-20. PubMed ID: 10674161 [Abstract] [Full Text] [Related]
12. Another case of 9P-syndrome. Mulcahy MT. Ann Genet; 1978 Mar; 21(1):47-9. PubMed ID: 308342 [Abstract] [Full Text] [Related]
15. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20. Okada M, Usami A, Okajima K, Yamada M, Yamaguchi Y, Umezaki I, Matsuda Y, Ohta H. Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498 [Abstract] [Full Text] [Related]