D. Bick

发表

Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts

Dagmar, Stavropoulos, J., 1998 .

Differential expression of novel Gsα signal transduction protein cDNA species

S. Weissman, A. Swaroop, N. Agarwal, 1991 .

Differential expression of novel Gs alpha signal transduction protein cDNA species.

S. Weissman, A. Swaroop, N. Agarwal, 1991, Nucleic acids research.

Prenatal diagnosis of Smith–Lemli–Opitz syndrome in a pregnancy with low maternal serum oestriol and a sex‐reversed fetus

R. Kelley, G. Berkovitz, H. Stern, 1999, Prenatal diagnosis.

Pathogenic variants in glutamyl-tRNAGln amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder

Pedro Rebelo-Guiomar, M. Minczuk, J. Veltman, 2018, Nature Communications.

Molecular analysis of the Rh locus in a person with the Du phenotype

A. Maddalena, W. Spence, D. Bick, 1994, Transfusion.

Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome.

D. Pfaff, D. Bick, M. Schwanzel‐Fukuda, 1989, Brain research. Molecular brain research.

Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay.

P. Hindmarsh, W. Crowley, D. Bick, 1999, The Journal of clinical endocrinology and metabolism.

Bringing Kallmann syndrome into focus.

A. Ballabio, D. Bick, D. Bick, 1993, AJNR. American journal of neuroradiology.