L. Christ

The structure and evolution of centromeric transition regions within the human genome

D. Haussler, E. Eichler, J. Bailey, 2004, Nature.

Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.

S. Schwartz, L. Christ, J. Conroy, 1999, American journal of human genetics.

Delineation of complex chromosomal rearrangements: evidence for increased complexity

S. Schwartz, L. Christ, B. Pletcher, 2004, Human Genetics.

Detection of deletions in de novo “balanced” chromosome rearrangements: Further evidence for their role in phenotypic abnormalities

E. Eichler, S. Schwartz, L. Christ, 2004, Genetics in Medicine.

Familial 9q22.3 microduplication spanning PTCH1 causes short stature syndrome with mild intellectual disability and dysmorphic features

L. Christ, D. Neilson, K. Izumi, 2011, American journal of medical genetics. Part A.

Characterization of a familial balanced rec(13) in a child with mild MR and his half‐sibling with two structurally rearranged chromosomes 13

S. Schwartz, L. Christ, L. Jeng, 2005, American journal of medical genetics. Part A.

Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: Genotype–phenotype correlations

L. Christ, T. Slavin, A. Mitchell, 2011, American journal of medical genetics. Part A.

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study

S. Schwartz, U. Surti, L. Christ, 2006, Journal of Medical Genetics.