111 related articles for article (PubMed ID: 16646109)
1. [Chromosome 1q syndrome and hearing loss: an unusual case].
Schwemmle C; Schulze B; Ptok M
Laryngorhinootologie; 2006 Apr; 85(4):279-82. PubMed ID: 16646109
[TBL] [Abstract][Full Text] [Related]
2. A case of deletion of the short arm of chromosome 10 with severe hearing loss and brainstem dysfunction.
Kinoshita Y; Tanaka Y; Yasuhara A; Matsuzaki S; Kuriki H; Kobayashi Y
Am J Perinatol; 1992 Jul; 9(4):299-301. PubMed ID: 1627224
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Proximal interstitial 1p36 deletion syndrome: the most proximal 3.5-Mb microdeletion identified on a dysmorphic and mentally retarded patient with inv(3)(p14.1q26.2).
Shimojima K; Páez MT; Kurosawa K; Yamamoto T
Brain Dev; 2009 Sep; 31(8):629-33. PubMed ID: 18835671
[TBL] [Abstract][Full Text] [Related]
5. [Chromosome 5q-syndrome-ENT pathologies].
Harréus UA; Issing WJ
Laryngorhinootologie; 2002 Aug; 81(8):565-7. PubMed ID: 12189572
[TBL] [Abstract][Full Text] [Related]
6. Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q.
Steinbach P; Wolf M; Schmidt H
Am J Med Genet; 1984 Sep; 19(1):131-6. PubMed ID: 6496565
[TBL] [Abstract][Full Text] [Related]
7. Interstitial deletion of 4p15.32p16.3 in a boy with minor anomalies, hearing loss, borderline intelligence, and oligodontia.
Kozma C; Chong SS; Meck JM
Am J Med Genet; 1999 Oct; 86(4):316-20. PubMed ID: 10494085
[TBL] [Abstract][Full Text] [Related]
8. Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypes.
Lin AE; Garver KL; Diggans G; Clemens M; Wenger SL; Steele MW; Jones MC; Israel J
Am J Med Genet; 1988 Nov; 31(3):533-48. PubMed ID: 3067575
[TBL] [Abstract][Full Text] [Related]
9. Partial monosomy of chromosome 2. Delineable syndrome of deletion 2 (q23-q31).
Shabtai F; Klar D; Halbrecht I
Ann Genet; 1982; 25(3):156-8. PubMed ID: 6982665
[TBL] [Abstract][Full Text] [Related]
10. A specific syndrome due to deletion of the distal long arm of chromosome 1.
Meinecke P; Vögtel D
Am J Med Genet; 1987 Oct; 28(2):371-6. PubMed ID: 3322005
[TBL] [Abstract][Full Text] [Related]
11. Phenotypic variability of del(2) (q22-q23): report of a case with a review of the literature.
Lurie IW; Supovitz KR; Rosenblum-Vos LS; Wulfsberg EA
Genet Couns; 1994; 5(1):11-4. PubMed ID: 8031530
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Tricho-rhino-phalangeal syndrome type I with severe mental retardation due to interstitial deletion of 8q23.3-24.13.
Yamamoto Y; Oguro N; Miyao M; Yanagisawa M
Am J Med Genet; 1989 Jan; 32(1):133-5. PubMed ID: 2784939
[TBL] [Abstract][Full Text] [Related]
14. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
15. Gardner syndrome in a boy with interstitial deletion of the long arm of chromosome 5.
Kobayashi T; Narahara K; Yokoyama Y; Ueyama S; Mohri O; Fujii T; Fujimoto M; Ohtsuki S; Tsuji K; Seino Y
Am J Med Genet; 1991 Dec; 41(4):460-3. PubMed ID: 1776638
[TBL] [Abstract][Full Text] [Related]
16. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
[TBL] [Abstract][Full Text] [Related]
17. Constitutional interstitial deletion of 17(p11.2) (Smith-Magenis syndrome): a clinically recognizable microdeletion syndrome. Report of two cases and review of the literature.
Fischer H; Oswald HP; Duba HC; Doczy L; Simma B; Utermann G; Haas OA
Klin Padiatr; 1993; 205(3):162-6. PubMed ID: 8350589
[TBL] [Abstract][Full Text] [Related]
18. Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q.
Thomas JA; Manchester DK; Prescott KE; Milner R; McGavran L; Cohen MM
Am J Med Genet; 1996 Apr; 62(4):372-5. PubMed ID: 8723067
[TBL] [Abstract][Full Text] [Related]
19. Van der Woude syndrome with mental retardation: case report.
Ugwu BT; Momoh JT
East Afr Med J; 2001 Feb; 78(2):111-2. PubMed ID: 11682943
[TBL] [Abstract][Full Text] [Related]
20. Interstitial deletion of (17)(p11.2p11.2) in nine patients.
Smith AC; McGavran L; Robinson J; Waldstein G; Macfarlane J; Zonona J; Reiss J; Lahr M; Allen L; Magenis E
Am J Med Genet; 1986 Jul; 24(3):393-414. PubMed ID: 2425619
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
