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7. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p. Leichtman LG; Zackowski JL; Storto PD; Newlin A Am J Med Genet; 1996 Jun; 63(3):434-7. PubMed ID: 8737648 [TBL] [Abstract][Full Text] [Related]
8. De novo tandem duplication 9p (p12----p24) with normal GALT activity in red cells. Motegi T; Watanabe K; Nakamura N; Hasegawa T; Yanagawa Y J Med Genet; 1985 Feb; 22(1):64-6. PubMed ID: 2984424 [TBL] [Abstract][Full Text] [Related]
9. Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review. El Khattabi L; Jaillard S; Andrieux J; Pasquier L; Perrin L; Capri Y; Benmansour A; Toutain A; Marcorelles P; Vincent-Delorme C; Journel H; Henry C; De Barace C; Devisme L; Dubourg C; Demurger F; Lucas J; Belaud-Rotureau MA; Amiel J; Malan V; De Blois MC; De Pontual L; Lebbar A; Le Dû N; Germain DP; Pinard JM; Pipiras E; Tabet AC; Aboura A; Verloes A Am J Med Genet A; 2015 Jun; 167(6):1252-61. PubMed ID: 25847481 [TBL] [Abstract][Full Text] [Related]
10. Moving towards a syndrome: a review of 20 cases and a new case of non-mosaic tetrasomy 9p with long-term survival. Tonk VS Clin Genet; 1997 Jul; 52(1):23-9. PubMed ID: 9272709 [TBL] [Abstract][Full Text] [Related]
11. [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; 26(2):103-5. PubMed ID: 6604482 [TBL] [Abstract][Full Text] [Related]
13. Tissue limited mosaicism in a patient with tetrasomy 9p. Papenhausen P; Riscile G; Miller K; Kousseff B; Tedesco T Am J Med Genet; 1990 Nov; 37(3):388-91. PubMed ID: 2260570 [TBL] [Abstract][Full Text] [Related]
14. Gene dosage studies supporting localization of the structural gene for galactose-1-phosphate uridyl transferase (GALT) to band p13 of chromosome 9. Shih LY; Suslak L; Rosin I; Searle BM; Desposito F Am J Med Genet; 1984 Nov; 19(3):539-43. PubMed ID: 6095663 [TBL] [Abstract][Full Text] [Related]
15. Mental retardation and congenital malformations associated with a ring chromosome 9. Nakajima S; Yanagisawa M; Kamoshita S; Nakagome Y Hum Genet; 1976 Jun; 32(3):289-93. PubMed ID: 939548 [TBL] [Abstract][Full Text] [Related]
16. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9. Shapiro SD; Hansen KL; Littlefield CA Am J Med Genet; 1985 Feb; 20(2):271-6. PubMed ID: 3976720 [TBL] [Abstract][Full Text] [Related]
17. Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance. Dallaire L J Med Genet; 1969 Jun; 6(2):113-20. PubMed ID: 4389828 [No Abstract] [Full Text] [Related]
18. Mosaic tetrasomy 12p. Gilgenkrantz S; Droulle P; Schweitzer M; Foliguet B; Chadefaux B; Lombard M; Chery M; Prieur M Clin Genet; 1985 Dec; 28(6):495-502. PubMed ID: 2934184 [TBL] [Abstract][Full Text] [Related]