M. Bar

Homozygous microdeletion of the POU1F1, CHMP2B, and VGLL3 genes in chromosome 3—A novel syndrome

M. Phillip, L. Lazar, G. Gat-Yablonski, 2011, American journal of medical genetics. Part A.

A novel loss-of-function mutation in GPR54/KISS1R leads to hypogonadotropic hypogonadism in a highly consanguineous family.

M. Phillip, R. Nimri, N. de Roux, 2011, The Journal of clinical endocrinology and metabolism.

Growth without Growth Hormone and Similar Dysmorphic Features in Three Patients with Sporadic Combined Pituitary Hormone Deficiencies

M. Phillip, L. de Vries, L. Lazar, 2009, Hormone Research in Paediatrics.