255 related articles for article (PubMed ID: 9950372)
1. De novo 10q22 interstitial deletion.
Cook L; Weaver DD; Hartsfield JK; Vance GH
J Med Genet; 1999 Jan; 36(1):71-2. PubMed ID: 9950372
[TBL] [Abstract][Full Text] [Related]
2. A case with de novo interstitial deletion of chromosome 7q21.1-q22.
Manguoğlu E; Berker-Karaüzüm S; Baumer A; Mihçi E; Taçoy S; Lüleci G; Schinzel A
Genet Couns; 2005; 16(2):155-9. PubMed ID: 16080295
[TBL] [Abstract][Full Text] [Related]
3. Interstitial deletion of bands 11q21-->22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes.
Horelli-Kuitunen N; Gahmberg N; Eeva M; Palotie A; Järvelä I
Am J Med Genet; 1999 Oct; 86(5):416-9. PubMed ID: 10508981
[TBL] [Abstract][Full Text] [Related]
4. Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion.
Tzschach A; Krause-Plonka I; Menzel C; Knoblauch A; Toennies H; Hoeltzenbein M; Radke M; Ropers HH; Kalscheuer V
Am J Med Genet A; 2006 May; 140(10):1108-10. PubMed ID: 16619204
[TBL] [Abstract][Full Text] [Related]
5. Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literature.
Wakazono A; Masuno M; Yamaguchi S; Tsubouchi K; Kondo N; Orii T
Jpn J Hum Genet; 1992 Sep; 37(3):229-34. PubMed ID: 1472705
[TBL] [Abstract][Full Text] [Related]
6. An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.
Bremer A; Schoumans J; Nordenskjöld M; Anderlid BM; Giacobini M
Eur J Med Genet; 2009; 52(5):358-62. PubMed ID: 19576304
[TBL] [Abstract][Full Text] [Related]
7. Interstitial deletion of 4(q21q25) in a liveborn male.
Rose NC; Schneider A; McDonald-McGinn DM; Caserta C; Emanuel BS; Zackai EH
Am J Med Genet; 1991 Jul; 40(1):77-9. PubMed ID: 1887853
[TBL] [Abstract][Full Text] [Related]
8. Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.
Zenger-Hain JL; Roberson J; Van Dyke DL; Weiss L
Am J Med Genet; 1993 Jun; 46(4):438-40. PubMed ID: 7689299
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Infant with multiple congenital anomalies and deletion (9)(q34.3).
Schimmenti LA; Berry SA; Tuchman M; Hirsch B
Am J Med Genet; 1994 Jun; 51(2):140-2. PubMed ID: 7522397
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The 4q-Syndrome.
Strehle EM; Ahmed OA; Hameed M; Russell A
Genet Couns; 2001; 12(4):327-39. PubMed ID: 11837601
[TBL] [Abstract][Full Text] [Related]
13. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
[TBL] [Abstract][Full Text] [Related]
14. De novo deletion of 1q31.1-q32.1 in a patient with developmental delay and behavioral disorders.
Milani D; Bedeschi MF; Iascone M; Chiarelli G; Cerutti M; Menni F
Cytogenet Genome Res; 2012; 136(3):167-70. PubMed ID: 22398643
[TBL] [Abstract][Full Text] [Related]
15. Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s.
Wenger SL; Boone LY; Cummins JH; Del Vecchio MA; Bay CA; Hummel M; Mowery-Rushton PA
Am J Med Genet; 2000 Apr; 91(5):351-4. PubMed ID: 10766997
[TBL] [Abstract][Full Text] [Related]
16. Girl with accelerated growth, hearing loss, inner ear anomalies, delayed myelination of the brain, and del(22)(q13.1q13.2).
Fujita Y; Mochizuki D; Mori Y; Nakamoto N; Kobayashi M; Omi K; Kodama H; Yanagawa Y; Abe T; Tsuzuku T; Yamanouchi Y; Takano T
Am J Med Genet; 2000 May; 92(3):195-9. PubMed ID: 10817654
[TBL] [Abstract][Full Text] [Related]
17. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
[TBL] [Abstract][Full Text] [Related]
18. Interstitial deletion of chromosome 18[del(18)(q11.2q12.2 or q12.2q21.1].
Surh LC; Ledbetter DH; Greenberg F
Am J Med Genet; 1991 Oct; 41(1):15-7. PubMed ID: 1719812
[TBL] [Abstract][Full Text] [Related]
19. De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability.
Brett MS; Ng IS; Lim EC; Yong MH; Li Z; Lai A; Tan EC
Gene; 2013 Mar; 517(1):82-8. PubMed ID: 23313878
[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]
