Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR

We recently studied a patient who meets criteria for autistic disorder and has a 2q37 deletion. Molecular cytogenetic studies were carried out using DNA isolated from 22 different 2q37 mapped BACs to more precisely define the extent of the chromosome deletion. We also analyzed 2q37 mapped polymorphi...

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Veröffentlicht in:	Cytogenetic and genome research 2001-01, Vol.94 (1-2), p.15-22
Hauptverfasser:	Smith, M., Escamilla, J.R., Filipek, P., Bocian, M.E., Modahl, C., Flodman, P., Spence, M.A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Autistic Disorder - complications Autistic Disorder - genetics Autistic Disorder - physiopathology Biological and medical sciences Bone and Bones - metabolism Bone Diseases - complications Bone Diseases - genetics Brain - metabolism Child Child, Preschool chromosome 2 Chromosome Deletion Chromosomes, Artificial, Bacterial Chromosomes, Human, Pair 2 - genetics Contig Mapping DNA Probes Female Fundamental and applied biological sciences. Psychology Gene Deletion Genes. Genome Genetic Markers - genetics Humans In Situ Hybridization, Fluorescence Male Microsatellite Repeats - genetics Molecular and cellular biology Molecular genetics Original Article Polymorphism, Genetic - genetics Psychometrics
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