Ring-20-syndrome and loss of telomeric regions

Annales de Genetique

Volumn 43, Issue 3-4, 2000, Pages 113-116

  García Cruz, Diana ^a   Isabel Vásquez, Ana ^a   Perez Rulfo, Daniel ^c   Omayra Dávalos, Nory ^a   Manuel Peñaloza, José ^a   Elías García Ortiz, José ^a   Patiño García, Brenda ^a   Sánchez Corona, José ^a,b  

^a UNIVERSITY OF GUADALAJARA   (Mexico)

^b CENTRO DE INVESTIGACIÓN BIOMÉDICA DE OCCIDENTE   (Mexico)

^c HOSPITAL DE PEDIATRÍA   (Mexico)

Author keywords

Mental retardation; Refractory epilepsy; Ring 20 chromosome; Syndrome; Telomeric sequences

Indexed keywords

ANTICONVULSIVE AGENT; FELBAMATE;

ARTICLE; BEHAVIOR DISORDER; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME LOSS; EPILEPSY; FLUORESCENCE IN SITU HYBRIDIZATION; FOCAL EPILEPSY; HUMAN; KARYOTYPE 46,XY; MALE; MENTAL DEFICIENCY; RING CHROMOSOME; SYNDROME; TELOMERE; TONIC CLONIC SEIZURE;

EID: 0034519833     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0003-3995(00)01027-3     Document Type: Article

References (21)

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5. Chromosome 20 ring: A chromosomal disorder associated with a particular electroclinical pattern
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11. Does 'ring syndrome' exist? An analysis of 207 case reports on patients with a ring autosome
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15. Report of two cases of distal deletion of the long arm of chromosome 6
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19. Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization
20. A study of ring 20 chromosome karyotype with epilepsy
21. Familiäres mosaik mit G-ring