A. Mutirangura

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

D. Ledbetter, S. Malcolm, M. Butler, 1993, Human molecular genetics.

Nondisjunction of chromosome 15: origin and recombination.

D. Ledbetter, S. Langlois, S. Malcolm, 1993, American journal of human genetics.

Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).

D. Ledbetter, J. Sutcliffe, A. Beaudet, 1994, Human molecular genetics.

A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene.

D. Ledbetter, J. Sutcliffe, A. Beaudet, 1993, Genomics.

PATHOMECHANISM OF X-LINKED OSTEOGENESIS IMPERFECTA Miss Siraprapa Tongkobpetch A Dissertation Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Program in Biomedical Sciences

S. Tongkobpetch, Thai Abst Ract, Apiwat Mutirangura, 2017 .

Dinucleotide repeat polymorphism at the GABAA receptor β3 (GABRB3) locus in the Angelman/Prader— Willi region (AS/PWS) of chromosome 15

D. Ledbetter, A. C. Chinault, A. Kuwano, 1992 .

Molecular and clinical study of 61 Angelman syndrome patients.

Y. Fukushima, N. Niikawa, S. Saitoh, 1994, American journal of medical genetics.

Wilms tumor in a patient with Prader-Willi syndrome.

D. Ledbetter, R. Weksberg, M. Coppes, 1993, The Journal of pediatrics.