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Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1993
Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosomeN Abbas, K McElreavey, M Leconiat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 1, 1994
[Pneumothorax revealing pneumoblastoma in an infant]A Paupe, H Martelli, R Lenclen, et al.
The Journal of Clinical Endocrinology and Metabolism|January 1, 1989
No evidence for a defect in growth hormone binding to liver membranes in thalassemia majorM C Postel-Vinay, R Girot, J Leger, et al.
Thrombosis and Haemostasis|February 28, 1983
Albumin, fibrinogen, prothrombin and antithrombin III variations in blood, urines and liver in rat nephrotic syndrome (Heymann nephritis)R Girot, F Jaubert, M Leon, et al.
Histopathology|April 2, 1998
Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's roleJ Rahier, C Sempoux, J C Fournet, et al.
The Journal of Pediatrics|November 1, 1994
True hermaphroditism: genetic variants and clinical managementC G Hadjiathanasiou, R Brauner, S Lortat-Jacob, et al.
Genes, Chromosomes & Cancer|July 1, 1993
FLT4 receptor tyrosine kinase gene mapping to chromosome band 5q35 in relation to the t(2;5), t(5;6), and t(3;5) translocationsE Armstrong, K Kastury, O Aprelikova, et al.
Genomics|April 15, 1997
Deletions of distal 9p associated with 46,XY male to female sex reversal: definition of the breakpoints at 9p23.3-p24.1R Veitia, M Nunes, R Brauner, et al.
Annales D'Endocrinologie|January 1, 1994
[Study of sex determination gene (SRY) in 46,XY gonadal dysgenesis]C Boucekkine, E Vilain, K McElreavey, et al.
Pediatric Radiology|April 14, 1999
CT scan patterns of pulmonary alveolar proteinosis in childrenV Albafouille, N Sayegh, S De Coudenhove, et al.
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