P Bouloux

Association of Parathyroid Tumors in Multiple Endocrine Neoplasia Type 1 with Loss of Alleles on Chromosome 11

Rajesh V. Thakker, P Bouloux, C Wooding et al. · New England Journal of Medicine · 1989 · 338 citations

Pancreatic Tumors, Men-1 Gene, Genetic Disorder +11

Xp22.3 deletions in isolated familial Kallmann's syndrome.

Jean‐Pierre Hardelin, Jacqueline Levilliers, Jacques Young et al. · The Journal of Clinical Endocrinology & Metabolism · 1993 · 102 citations

Developmental Anomaly, Developmental Biology, Mendelian Disorder +14

Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.

Alfons Meindl, D. Hosenfeld, W Bruckl et al. · Journal of Medical Genetics · 1993 · 49 citations · Full text

Linkage analysis of 7 polymorphic markers at chromosome 11p11. 2‐11q13 in 27 multiple endocrine neoplasia type 1 families

Rajesh V. Thakker, C Wooding, J T Pang et al. · Annals of Human Genetics · 1993 · 30 citations

Cancer Pathology, Genetics, Genetic Epidemiology +19

Expression of Gonadotropin-Releasing Hormone Type-I (GnRH-I) and Type-II (GnRH-II) in Human Peripheral Blood Mononuclear Cells (PMBCs) and Regulation of B-Lymphoblastoid Cell Proliferation by GnRH-I and GnRH-II

David González-Martı́nez, Letícia Ferreira Gontijo Silveira, Yijie Hu et al. · Experimental and Clinical Endocrinology & Diabetes · 2004 · 18 citations