M. Crumley

发表

Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene.

C. Langman, N. Roslin, K. Morgan, 2001, Journal of the American Society of Nephrology : JASN.

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

C. Greenberg, T. Weiler, K. Morgan, 1998, American journal of human genetics.

Identity-by-descent sharing using Markov chain Monte Carlo in subsets of the asthma Hutterite pedigree

D. Goldstein, A. Bureau, C. Greenwood, 2001 .

Pedigree Selection and Tests of Linkage in a Hutterite Asthma Pedigree

Alexandre Bureau, D. Goldstein, A. Bureau, 2001, Genetic epidemiology.

Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approach.

D. Housman, V. Stanton, P. Gros, 1995, Genomics.

Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidus.

D. Bichet, S. Sasaki, S. Sasaki, 2000, Journal of the American Society of Nephrology : JASN.

Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci.

C. Greenberg, W. Halliday, T. Weiler, 1997, American journal of medical genetics.

Identity Development of Adolescent Gay Black Males

M. Crumley, 2013 .

Bowen–Conradi syndrome: A clinical and genetic study

F. Bernier, A. Innes, C. Greenberg, 2003, American journal of medical genetics. Part A.