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The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defectsC Beldjord, F Desclaux-Arramond, M Raffin-Sanson, et al.
Nouvelle Revue Francaise D'Hematologie; Blood Cells|January 1, 1977
[A new case of hemoglobin J Capetown alpha 92 (FG 4) Arg replaced by gln]G Gacon, K E Amegnizin, O Belkhodja, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Haemoglobin D-Ouled Rabah among the Mozabites: a relevant variant to trace the origin of Berber-speaking populationsT Merghoub, A Sanchez-Mazas, R Tamouza, et al.
Blood|April 1, 1987
The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF levelR L Nagel, S K Rao, O Dunda-Belkhodja, et al.
Annales De Genetique|May 20, 2000
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardationP Billuart, J Chelly, A Carrié, et al.
Nouvelle Revue Francaise D'Hematologie|October 1, 1994
Fetal haemoglobin variations following hydroxyurea treatment in patients with cyanotic congenital heart diseaseP Triadou, M Maier-Redelsperger, R Krishnamoorty, et al.
Clinical Genetics|May 15, 2015
X-chromosome inactivation in female patients with Fabry diseaseL Echevarria, K Benistan, A Toussaint, et al.
Human Genetics|May 1, 1992
A novel sickle cell mutation of yet another origin in Africa: the Cameroon typeC Lapouméroulie, O Dunda, R Ducrocq, et al.
American Journal of Human Genetics|April 1, 1997
A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1996
[Closed spinal dysraphism. Apropos of 3 cases]L Benzekri, R Jarmouni, K Zouhair, et al.
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