Chen‐Chi Lee

Chromosome Abnormalities and Genetic Counseling

Identification of genes in toxicity pathways of trinucleotide-repeat RNA in C. elegans

RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression

FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism

Lymphedema beyond breast cancer

Health Supervision for Children With Down Syndrome

Revised American Thyroid Association Guidelines for the Management of Medullary Thyroid Carcinoma

Medullary Thyroid Cancer: Management Guidelines of the American Thyroid Association

Cancer Genetic Testing and Assisted Reproduction

Gene Duplication: A Drive for Phenotypic Diversity and Cause of Human Disease

Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera

Prenatal diagnosis of premature centromere division–related mosaic variegated aneuploidy

Prenatal diagnosis ofde novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertainedde novo apparently balanced complex and multiple chromosomal rearrangements

Prenatal diagnosis of interstitially satellited 6p

Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q

Successful triplet pregnancy and delivery after oocyte donation in an infertile female with chromosome mosaicism for monosomy X, partial trisomy X, and terminal Xp deletion

Cytogenetic evaluation of cystic hygroma associated with hydrops fetalis, oligohydramnios or intrauterine fetal death: the roles of amniocentesis, postmortem chorionic villus sampling and cystic hygroma paracentesis

Isochromosome 18q in a fetus with congenital megacystis, intra-uterine growth retardation and cloacal dysgenesis sequence