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2. Coincidence of paternal 13pYq translocation and maternal increased 13p NOR activity in a child with arthrogryposis and other malformations. Bajnóczky K; Meggyessy V Acta Paediatr Hung; 1985; 26(2):151-6. PubMed ID: 4041282 [TBL] [Abstract][Full Text] [Related]
3. Arthrogryposis-like signs in trisomy 18. Lambert JC; Ferrari M; Donzeau M; Ayraud N; Chiaramello W; Mariani R Hum Genet; 1981; 57(2):145-7. PubMed ID: 7228025 [TBL] [Abstract][Full Text] [Related]
4. Duplication of 16q and deletion of 15q. Nyhan WL; Mascarello J; Barshop B; Doroski D; Hirschhorn K Am J Med Genet; 1989 Oct; 34(2):183-6. PubMed ID: 2816995 [TBL] [Abstract][Full Text] [Related]
5. Amyoplasia associated with a balanced de novo insertion of a segment of the long arm of chromosome 5 into chromosome 2. Eisenhut M; Weindling M; Fryer A Am J Med Genet; 2002 Feb; 107(4):337-9. PubMed ID: 11840493 [No Abstract] [Full Text] [Related]
6. Maternal translocation t(13:18)(q34:q11) and Edward's syndrome in a fetus: 47,xy,t(13:18)(q34:q11) + 18. Marković S; Boué J; Krstić M; Sulović V; Dozić S; Adzić S Clin Genet; 1984 Nov; 26(5):481-4. PubMed ID: 6499261 [TBL] [Abstract][Full Text] [Related]
7. A child with partial trisomy of chromosome 17 and partial monosomy of chromosome 3: 46,XY,der(3),t(3;17)(p25;q23). Shawe DJ; Fear C; Appleyard WJ J Med Genet; 1983 Oct; 20(5):383-5. PubMed ID: 6196484 [TBL] [Abstract][Full Text] [Related]
8. Three distinct types of X-linked arthrogryposis seen in 6 families. Hall JG; Reed SD; Scott CI; Rogers JG; Jones KL; Camarano A Clin Genet; 1982 Feb; 21(2):81-97. PubMed ID: 7200838 [TBL] [Abstract][Full Text] [Related]
10. [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]
11. Segregation of two independent chromosomal translocations in one family. Miller K; Flatz SD Hum Genet; 1984; 68(1):93-5. PubMed ID: 6500562 [TBL] [Abstract][Full Text] [Related]
12. A 46,XY, del(18)(pter leads to p1 100:) cebocephalic child from a 46,XX,t(12;18)(18pter leads to 18 p 1100:: 12qter leads to 12pter) normal parent. Johnson G; Bachman R Hum Genet; 1976 Sep; 34(1):103-6. PubMed ID: 964998 [TBL] [Abstract][Full Text] [Related]
17. Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat. Stern LM; Mureh AR J Med Genet; 1975 Sep; 12(3):305-7. PubMed ID: 1177285 [TBL] [Abstract][Full Text] [Related]
18. Partial trisomy 18 in a family with a translocation (18;21)(q21;q22). Niazi M; Coleman DV; Saldaña-Garcia P J Med Genet; 1978 Apr; 15(2):148-51. PubMed ID: 641950 [TBL] [Abstract][Full Text] [Related]
19. A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter. Voss R; Gross-Kieselstein E; Hurvitz H; Dagan J; Kerem E; Zlotogora J J Med Genet; 1984 Dec; 21(6):454-9. PubMed ID: 6512835 [TBL] [Abstract][Full Text] [Related]