Effectiveness of posthumous molecular diagnosis from a kept baby tooth

Lancet

Volumn 366, Issue 9496, 2005, Pages 1584-

  Leonard, Helen ^a   Davis, Mark R ^b   Turbett, Gavin R ^c   Laing, Nigel G ^d   Bower, Carol ^a   Ravine, David ^e  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^b ROYAL PERTH HOSPITAL   (Australia)

^c Western Australian Centre for Pathology and Medical Research   (Australia)

^d UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^e UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ANTICONVULSIVE AGENT; METHYL CPG BINDING PROTEIN 2;

ARTICLE; CASE REPORT; CHILD; CHILD DEVELOPMENT; DIAGNOSTIC PROCEDURE; DNA EXTRACTION; FEMALE; FORENSIC MEDICINE; GENE MUTATION; GENE SEQUENCE; GENETIC RISK; HUMAN; HUMAN TISSUE; NEUROLOGIC DISEASE; NONSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; RETT SYNDROME; SEIZURE; TOOTH; X CHROMOSOMAL INHERITANCE;

EID: 27544514729     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(05)67631-3     Document Type: Article

References (5)

1. L Colvin, S Fyfe, S Leonard Describing the phenotype in Rett syndrome using a population database Arch Dis Child 88 2003 38 43
2. PS Walsh, DA Metzger, R Higuchi Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material Biotechniques 10 1991 506 513
3. J Christodoulou, A Grimm, T Maher, B Bennetts RettBASE: The IRSA MECP2 variation database - a new mutation database in evolution Hum Mutat 21 2003 466 472
4. U Moog, E Smeets, K Van Roozendaal Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2) Eur J Paediatr Neurol 7 2003 5 12
5. G Restagno, M Ferrone, C Doriguzzi, L Palmucci, T Mongini, A Carbonara Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected child Prenat Diagn 15 1995 672 674