M. G. Butler

Screen for MAOA mutations in target human groups.

D. Murphy, B. Greenberg, C. Schwartz, 1999, American journal of medical genetics.

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.

Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5.

J. Wasmuth, U. Bengtsson, J. Ulm, 1989, American journal of human genetics.

High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader-Willi or Angelman syndrome.

M. Butler, M. G. Butler, 1995, American journal of medical genetics.

Deficiency in prohormone convertase PC 1 impairs prohormone processing in Prader-Willi syndrome

C. Poitou, Daniel Paull, A. Skowronski, 2022 .

The use of skinfold measurements to judge obesity during the early phase of Prader-Labhart-Willi syndrome.

M. Butler, F. Meaney, R. Butler, 1988, International journal of obesity.

Klinefelter and trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15--a coincidence?

P. Rogan, J. Moeschler, M. Butler, 1997, American journal of medical genetics.

Focal sclerosing glomerulonephritis in a child with Laurence-Moon-Biedl syndrome.

M. Butler, A. Glick, A. Barakat, 1990, Child nephrology and urology.