Robert Wallerstein

The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome

Michael J. Bamshad, Thanh Le, W. Scott Watkins et al. · The American Journal of Human Genetics · 1999 · 177 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +12

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

Robert Wallerstein, Ming-Tsung Yu, Richard L. Neu et al. · Prenatal Diagnosis · 2000 · 124 citations

Cytogenetics, Genetics, Gynecology +20

Novel ITGB4 Mutations in Lethal and Nonlethal Variants of Epidermolysis Bullosa with Pyloric Atresia: Missense versus Nonsense

Leena Pulkkinen, Fatima Rouan, Leena Bruckner–Tuderman et al. · The American Journal of Human Genetics · 1998 · 116 citations · Full text

Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population.

Robert Wallerstein, Carol E. Anderson, Beverly N. Hay et al. · Journal of Medical Genetics · 1997 · 79 citations · Full text

Rubinstein-taybi Syndrome, Submicroscopic Deletions, Genetics +19

Outcome of prenatally diagnosed trisomy 6 mosaicism

Robert Wallerstein, Tracey Oh, Judy Durcan et al. · Prenatal Diagnosis · 2002 · 79 citations