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2. Langer-Giedion syndrome with interstitial 8q-deletion. Zabel BU; Baumann WA Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298 [TBL] [Abstract][Full Text] [Related]
3. Chromosome 11 long arm partial deletion: a new syndrome. Engel E; Hirshberg CS; Cassidy SB; McGee BJ Am J Ment Defic; 1976 Jan; 80(4):473-5. PubMed ID: 1247044 [TBL] [Abstract][Full Text] [Related]
4. The syndrome of ring chromosome 12. Scribanu N; McCullars EB; Baumiller RC; Colon AR Am J Med Genet; 1980; 5(2):165-70. PubMed ID: 7395909 [TBL] [Abstract][Full Text] [Related]
5. Ring chromosome 11 [46,XX,r(11) (p15q25)] associated with clinical features of the 11q- syndrome. Niikawa N; Jinno Y; Tomiyasu T; Fukushima Y; Kudo K Ann Genet; 1981; 24(3):172-5. PubMed ID: 6974530 [TBL] [Abstract][Full Text] [Related]
6. A case of deletion of short arm of chromosome 8. Leisti J; Aula P Birth Defects Orig Artic Ser; 1977; 13(3B):187-94. PubMed ID: 890091 [No Abstract] [Full Text] [Related]
7. A case of partial deletion of the long arm of chromosome 7 (7q34 leads to 7qter). Nistrup Madsen H; Lundsteen C; Steinrud J Dan Med Bull; 1983 Feb; 30(1):14-6. PubMed ID: 6831934 [No Abstract] [Full Text] [Related]
8. Partial trisomy 8 mosaicism with 46,XX/46,XX-8,+dic(8). Ray M; Hunter AG Ann Genet; 1980; 23(2):100-2. PubMed ID: 6967279 [TBL] [Abstract][Full Text] [Related]
9. [Prenatal diagnosis of a de novo trisomy case 9q-47,XX,+9 del(q33----qter)]. Cordier MP; Coicaud C; Thoulon JM; Robert JM; Germain D J Genet Hum; 1984 Dec; 32(5):351-61. PubMed ID: 6527131 [TBL] [Abstract][Full Text] [Related]
10. Case report of mosaic partial tetrasomy 9 mimicking Klinefelter syndrome. Peters J; Pehl C; Miller K; Sandlin CJ Birth Defects Orig Artic Ser; 1982; 18(3B):287-93. PubMed ID: 7139111 [No Abstract] [Full Text] [Related]
11. 10p-: a new autosomal deletion syndrome? Francke U; Mahan GM; Dixson BK; Jones OW Birth Defects Orig Artic Ser; 1975; 11(5):207-12. PubMed ID: 1218215 [No Abstract] [Full Text] [Related]
12. Partial deletion of the short arm of a chromosome No. 4. Wolf's syndrome. van Kempen C; Jongbloet PH Maandschr Kindergeneeskd; 1967 Oct; 35(8):252-69. PubMed ID: 6065161 [No Abstract] [Full Text] [Related]
13. Malformation syndrome of duplication 12q24.1 leads to qter. Melnyk AR; Weiss L; Van Dyke DL; Jarvi P Am J Med Genet; 1981; 10(4):357-65. PubMed ID: 7332029 [TBL] [Abstract][Full Text] [Related]
14. [The follow-up of a child with a syndrome due to partial deletion of chromosome 3 (p25-pter)]. Tucciarone L; Tomassini A; Colasanti A; Sabbi T; Stella P Minerva Pediatr; 1999; 51(7-8):283-8. PubMed ID: 10634062 [TBL] [Abstract][Full Text] [Related]
15. [Partial deletion of the short arm of chromosome 4 (the Wolf-Hirschhorn syndrome) with reference to the neurological and electroencephalographic aspects]. Bonaventura F; Adamoli P; Bernardini E; Branchi M; Siani A; Bonora G Pediatr Med Chir; 1994; 16(4):393-8. PubMed ID: 7816704 [TBL] [Abstract][Full Text] [Related]
16. New chromosomal malformation syndromes. I. Partial monosomy 8p. An attempt to establish a new chromosome deletion syndrome. Rodewald A; Stengel-Rutkowski S; Schulz P; Cleve H Eur J Pediatr; 1977 Apr; 125(1):45-57. PubMed ID: 870324 [TBL] [Abstract][Full Text] [Related]
17. Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemia. Werner-Favre C; Cabrol C; Beris P; Engel E Ann Genet; 1983; 26(4):240-2. PubMed ID: 6607706 [TBL] [Abstract][Full Text] [Related]
18. [Partial deletion of the short arm of chromosome 8]. Bresson JL; Noir A; Scherrer M Ann Genet; 1977 Mar; 20(1):70-2. PubMed ID: 302680 [TBL] [Abstract][Full Text] [Related]
19. Further delineation of the 10p deletion syndrome. Elstner CL; Carey JC; Livingston G; Moeschler J; Lubinsky M Pediatrics; 1984 May; 73(5):670-5. PubMed ID: 6718125 [TBL] [Abstract][Full Text] [Related]