132 related articles for article (PubMed ID: 8721571)
1. Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delay.
Aalfs CM; Jacobs ME; Nieste-Otter MA; Hennekam RC; Hoovers JM
Clin Genet; 1996 Jan; 49(1):42-5. PubMed ID: 8721571
[TBL] [Abstract][Full Text] [Related]
2. Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH.
Stankiewicz P; Bocian E; Jakubów-Durska K; Obersztyn E; Lato E; Starke H; Mroczek K; Mazurczak T
J Med Genet; 2000 Feb; 37(2):114-20. PubMed ID: 10662811
[TBL] [Abstract][Full Text] [Related]
3. Supernumerary chromosome marker (1) in a developmentally delayed child.
Lanphear N; Lamb A; Oppenheimer S; Soukup S
Am J Med Genet; 1995 Jul; 57(3):400-2. PubMed ID: 7545867
[TBL] [Abstract][Full Text] [Related]
4. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
[TBL] [Abstract][Full Text] [Related]
5. Mosaicism for a small supernumerary ring X chromosome in a dysmorphic, growth-retarded male: mos47,XXY/48,XXY, +r(X).
Manea SR; Gershin IF; Babu A; Willner JP; Desnick RJ; Cotter PD
Clin Genet; 1997 Dec; 52(6):432-5. PubMed ID: 9520254
[TBL] [Abstract][Full Text] [Related]
6. Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.
Levy B; Jalal SM; Dunn TM; Warburton PE; Tonk VS; Hirschhorn K; Lockhart LH; Hughes T; Velagaleti GV
Am J Med Genet; 2002 Mar; 108(3):198-204. PubMed ID: 11891685
[TBL] [Abstract][Full Text] [Related]
7. Ring Chromosome 9 and Chromosome 9p Deletion Syndrome in a Patient Associated with Developmental Delay: A Case Report and Review of the Literature.
Sivasankaran A; Kanakavalli MK; Anuradha D; Samuel CR; Kandukuri LR
Cytogenet Genome Res; 2016; 148(2-3):165-73. PubMed ID: 27222354
[TBL] [Abstract][Full Text] [Related]
8. 10p duplication characterized by fluorescence in situ hybridization.
Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
[TBL] [Abstract][Full Text] [Related]
9. Autism and hypoplastic corpus callosum in a case of monocentric marker chromosome 15.
Jovanović-Privrodski JD; Kavecan II; Obrenović MR; Buonadonna LA; Bukvić NM
Pediatr Neurol; 2009 Jul; 41(1):65-7. PubMed ID: 19520280
[TBL] [Abstract][Full Text] [Related]
10. A patient with a de novo t (6;9) and an interstitial duplication of (9)(q21.2q22.1).
Mohrschladt MF; Bijlsma EK; Sluijter S; De Coo RF; Hoovers JM; Leschot NJ
Clin Dysmorphol; 1999 Jul; 8(3):211-4. PubMed ID: 10457857
[TBL] [Abstract][Full Text] [Related]
11. Supernumerary der(1) marker chromosome derived from a ring chromosome 1 which has retained the original centromere and euchromatin from 1q21.1 --> q21.3 with substantial loss of 1q12 heterochromatin in a female with dysmorphic features and psychomotoric developmental delay.
Barbi G; Spaich Ch; Adolph S; Rossier E; Kehrer-Sawatzki H
Am J Med Genet A; 2005 Feb; 132A(4):419-24. PubMed ID: 15633178
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay.
Chen CP; Chiang S; Wang KL; Cho FN; Chen M; Chern SR; Wu PS; Chen YN; Chen SW; Chang SP; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2016 Jun; 55(3):419-22. PubMed ID: 27343327
[TBL] [Abstract][Full Text] [Related]
13. A boy with small supernumerary marker chromosome X identified by FISH.
Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
[TBL] [Abstract][Full Text] [Related]
14. Two supernumerary marker chromosomes, originating from chromosomes 6 and 11, in a child with developmental delay and craniofacial dysmorphism.
Maurer B; Haaf T; Stout K; Reissmann N; Steinlein C; Schmid M
Cytogenet Cell Genet; 2001; 93(3-4):182-7. PubMed ID: 11528110
[TBL] [Abstract][Full Text] [Related]
15. Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies.
Melnyk AR; Dewald G
Am J Med Genet; 1994 Mar; 50(1):12-4. PubMed ID: 7512788
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a chromosome 8-derived minute marker chromosome using microdissection and FISH in a boy with growth retardation.
Engelen JJ; Schrander-Stumpel CT; Theunissen PM; Vaes-Peeters G; Albrechts JC; Hamers AJ
Am J Med Genet A; 2003 Apr; 118A(3):274-8. PubMed ID: 12673659
[TBL] [Abstract][Full Text] [Related]
17. Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.
Abuelo D; Mark HF; Bier JA
Clin Pediatr (Phila); 1995 Apr; 34(4):223-6. PubMed ID: 7540523
[No Abstract] [Full Text] [Related]
18. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
[TBL] [Abstract][Full Text] [Related]
19. A
Jeevan Kumar M; Gowrishankar K; Hemagowri V; Kadandale J
J Genet; 2020; 99():. PubMed ID: 33021245
[TBL] [Abstract][Full Text] [Related]
20. Marker chromosome 21 identified by microdissection and FISH.
Sun Y; Rubinstein J; Soukup S; Palmer CG
Am J Med Genet; 1995 Mar; 56(2):151-4. PubMed ID: 7542834
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]