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3. Brief clinical report: interstitial deletion of the long arm of chromosome 10: del(10)(q11.2q21). Holden JJ; MacDonald EA Am J Med Genet; 1985 Feb; 20(2):245-8. PubMed ID: 2579554 [TBL] [Abstract][Full Text] [Related]
4. De novo interstitial deletion of the long arm of chromosome 7:46,XY,del(7)(q23;q32). Martin-Pont B; Pilczer C; Dandine M; Tamboise A Ann Genet; 1985; 28(4):251-3. PubMed ID: 3879441 [TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)]. Al-Awadi SA; Farag TI; Usha R; el-Khalifa MY; Sundareshan TS; Al-Othman SA Am J Med Genet; 1986 Apr; 23(4):931-3. PubMed ID: 3963055 [TBL] [Abstract][Full Text] [Related]
6. A case of interstitial 1q deletion [46,XY,del(q25q32.1)]. Hamano S; Fukushima Y; Yamada T; Shimizu H; Okuyama M; Ito F; Maekawa K Ann Genet; 1987; 30(2):105-8. PubMed ID: 3314663 [TBL] [Abstract][Full Text] [Related]
7. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3. Meng J; Fujita H; Nagahara N; Kashiwai A; Yoshioka Y; Funato M Am J Med Genet; 1992 Jul; 43(4):747-50. PubMed ID: 1621768 [TBL] [Abstract][Full Text] [Related]
8. Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH. Sukumar S; Wang S; Hoang K; Vanchiere CM; England K; Fick R; Pagon B; Reddy KS Am J Med Genet; 1999 Nov; 87(1):17-22. PubMed ID: 10528241 [TBL] [Abstract][Full Text] [Related]
9. Distal 12p deletion in a stillborn infant. Baroncini A; Avellini C; Neri C; Forabosco A Am J Med Genet; 1990 Jul; 36(3):358-60. PubMed ID: 2363438 [TBL] [Abstract][Full Text] [Related]
10. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3). Copelli S; del Rey G; Heinrich J; Coco R Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102 [TBL] [Abstract][Full Text] [Related]
11. Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patients. Tranebjaerg L; Nielsen KB; Tommerup N; Warburg M; Mikkelsen M Am J Med Genet; 1988 Apr; 29(4):739-53. PubMed ID: 3400720 [TBL] [Abstract][Full Text] [Related]
12. Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome. Courtens W; Speleman F; Messiaen L; Bormans J; Van Roy N; Vamos E Am J Med Genet; 1997 Sep; 71(4):479-85. PubMed ID: 9286460 [TBL] [Abstract][Full Text] [Related]
13. Del (8) (q212q2200) de novo in a boy without Langer-Giedion syndrome. Rivera H; Rodríguez RM; Plascencia ML; Martínez y Martínez R; Nazara Z; Cantu JM J Genet Hum; 1983 Dec; 31 Suppl 5():413-8. PubMed ID: 6674417 [TBL] [Abstract][Full Text] [Related]
14. Interstitial deletion of long arm of chromosome 13. Carnevale A; Frias S; Alcantar R Ann Genet; 1984; 27(1):49-52. PubMed ID: 6609673 [TBL] [Abstract][Full Text] [Related]
16. Deletion of the distal long arm of chromosome 1: a definable syndrome. Johnson VP; Heck LJ; Carter GA; Flom JO Am J Med Genet; 1985 Dec; 22(4):685-94. PubMed ID: 4073121 [TBL] [Abstract][Full Text] [Related]
17. [De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child]. Turleau C; Roubin M; Chavin-Colin F; Satge M; de Grouchy J Ann Genet; 1974 Dec; 17(4):291-4. PubMed ID: 4548828 [No Abstract] [Full Text] [Related]
18. Characterization of a 5.8-Mb interstitial deletion of chromosome 3p in a girl with 46,XX,inv(7)dn karyotype and phenotypic abnormalities. Morales C; Mademont-Soler I; Armengol L; Milà M; Badenas C; Andrés S; Soler A; Sánchez A Cytogenet Genome Res; 2009; 125(4):334-40. PubMed ID: 19864897 [TBL] [Abstract][Full Text] [Related]
19. De novo del(6)(q25) associated with macular degeneration. Rivas F; Ruiz C; Rivera H; Möller M; Serrano-Lucas JI; Cantú JM Ann Genet; 1986; 29(1):42-4. PubMed ID: 3487275 [TBL] [Abstract][Full Text] [Related]
20. Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12)(q24;q24). Callier P; Faivre L; Marle N; Thauvin-Robinet C; Mosca AL; Masurel-Paulet A; Borgnon J; Falcon-Eicher S; Danino A; Malka G; Le Merrer M; Huet F; Mugneret F Eur J Med Genet; 2007; 50(6):455-64. PubMed ID: 17720646 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]