L. Jenkins

Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.

S. Schwartz, F. Tsien, W. Flejter, 1994, American journal of human genetics.

Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype–phenotype correlations

L. Shaffer, S. Patil, C. Jackson-Cook, 2000, Prenatal diagnosis.

New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome.

J. Rosenfeld, B. Torchia, L. Shaffer, 2011, European journal of medical genetics.

Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations.

S. Schwartz, B. Sullivan, E. Karson, 1996, American journal of human genetics.

Transformation and establishment of fragile X cell lines from amniocytes.

D. Gruenert, E. Jenkins, L. Jenkins, 1991, American journal of medical genetics.

Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.

S. Schwartz, J. Leana-Cox, L. Jenkins, 1998, American journal of human genetics.

RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS

C L Bradshaw, L. Shaffer, C. Disteche, 1997, Prenatal diagnosis.

Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype–phenotype correlations

L. Shaffer, S. Patil, C. Jackson-Cook, 2000, Prenatal diagnosis.