337 related articles for article (PubMed ID: 16619204)
1. 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]
2. Molecular cytogenetic analysis of a de novo interstitial deletion of 5q23.3q31.2 and its phenotypic consequences.
Tzschach A; Krause-Plonka I; Menzel C; Kalscheuer V; Toennies H; Scherthan H; Knoblauch A; Radke M; Ropers HH; Hoeltzenbein M
Am J Med Genet A; 2006 Mar; 140(5):496-502. PubMed ID: 16470790
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies.
Gläser B; Rossier E; Barbi G; Chiaie LD; Blank C; Vogel W; Kehrer-Sawatzki H
Am J Med Genet A; 2003 Jan; 116A(1):66-70. PubMed ID: 12476454
[TBL] [Abstract][Full Text] [Related]
5. An interstitial deletion of chromosome 7 at band q21: a case report and review.
Courtens W; Vermeulen S; Wuyts W; Messiaen L; Wauters J; Nuytinck L; Peeters N; Storm K; Speleman F; Nöthen MM
Am J Med Genet A; 2005 Apr; 134A(1):12-23. PubMed ID: 15732063
[TBL] [Abstract][Full Text] [Related]
6. De Novo 1.77-Mb Microdeletion of 10q22.2q22.3 in a Girl With Developmental Delay, Speech Delay, Congenital Cleft Palate, and Bilateral Hearing Impairment.
Lei TY; Wang HT; Li F; Cui YQ; Fu F; Li R; Liao C
Cleft Palate Craniofac J; 2017 May; 54(3):343-350. PubMed ID: 27031267
[TBL] [Abstract][Full Text] [Related]
7. Rare interstitial deletion 9q31.2 to q33.1 de novo: longitudinal study in a patient over a period of more than 20 years.
Gamerdinger U; Eggermann T; Schubert R; Schwanitz G; Kreiss-Nachtsheim M
Am J Med Genet A; 2008 May; 146A(9):1180-4. PubMed ID: 18386807
[TBL] [Abstract][Full Text] [Related]
8. Molecular characterization of an 11q interstitial deletion in a patient with the clinical features of Jacobsen syndrome.
Wenger SL; Grossfeld PD; Siu BL; Coad JE; Keller FG; Hummel M
Am J Med Genet A; 2006 Apr; 140(7):704-8. PubMed ID: 16502431
[TBL] [Abstract][Full Text] [Related]
9. A de novo interstitial deletion of chromosome 15 band q25 as revealed by FISH-technique.
Verma RS; Kleyman SM; Giridharan R; Ramesh KH
Clin Genet; 1996 Jun; 49(6):303-5. PubMed ID: 8884079
[TBL] [Abstract][Full Text] [Related]
10. Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies.
Petek E; Windpassinger C; Simma B; Mueller T; Wagner K; Kroisel PM
J Hum Genet; 2003; 48(6):283-287. PubMed ID: 12836054
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. De novo interstitial deletion 2q14.1q22.1: is there a recognizable phenotype?
Greally MT; Robinson E; Allen NM; O'Donovan D; Crolla JA
Am J Med Genet A; 2014 Dec; 164A(12):3194-202. PubMed ID: 25263257
[TBL] [Abstract][Full Text] [Related]
14. A report of three patients with an interstitial deletion of chromosome 15q24.
Cushman LJ; Torres-Martinez W; Cherry AM; Manning MA; Abdul-Rahman O; Anderson CE; Punnett HH; Thurston VC; Sweeney D; Vance GH
Am J Med Genet A; 2005 Aug; 137(1):65-71. PubMed ID: 16007617
[TBL] [Abstract][Full Text] [Related]
15. Distal deletion, del(2)(q33.3q33.3), in a patient with severe growth deficiency and minor anomalies.
Riegel M; Morava E; Czakó M; Kosztolányi G; Schinzel A
Am J Med Genet; 2001 Aug; 102(3):227-30. PubMed ID: 11484198
[TBL] [Abstract][Full Text] [Related]
16. Interstitial deletion of the long arm of chromosome 5 in a boy with multiple congenital anomalies and mental retardation: Molecular characterization of the deleted region to 5q22.3q23.3.
Garcia-Miñaur S; Ramsay J; Grace E; Minns RA; Myles LM; FitzPatrick DR
Am J Med Genet A; 2005 Feb; 132A(4):402-10. PubMed ID: 15742475
[TBL] [Abstract][Full Text] [Related]
17. Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37).
Gorski JL; Cox BA; Kyine M; Uhlmann W; Glover TW
Am J Med Genet; 1989 Mar; 32(3):350-2. PubMed ID: 2729355
[TBL] [Abstract][Full Text] [Related]
18. FISH and cytogenetic characterization of a terminal chromosome 1q deletion: clinical case report and phenotypic implications.
Gentile M; Di Carlo A; Volpe P; Pansini A; Nanna P; Valenzano MC; Buonadonna AL
Am J Med Genet A; 2003 Mar; 117A(3):251-4. PubMed ID: 12599188
[TBL] [Abstract][Full Text] [Related]
19. Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?
Rauen KA; Albertson DG; Pinkel D; Cotter PD
Am J Med Genet; 2002 Jun; 110(1):51-6. PubMed ID: 12116271
[TBL] [Abstract][Full Text] [Related]
20. De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia.
Magri C; Piovani G; Pilotta A; Michele T; Buzi F; Barlati S
Eur J Med Genet; 2011; 54(3):361-4. PubMed ID: 21211576
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
