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Annales De Genetique|January 1, 1987
[HLA and molar pregnancies (triploidies, hydatidiform moles and choriocarcinoma). Etiological and epidemiological study]P Couillin, N Ravisé, J M Afoutou, et al.
Somatic Cell and Molecular Genetics|November 1, 1989
Characterization of human IFN-gamma response using somatic cell hybrids of hematopoietic and nonhematopoietic originM R Bono, P Benech, P Couillin, et al.
The New England Journal of Medicine|July 25, 1985
Late-onset adrenal hyperplasia in hirsutismF Kuttenn, P Couillin, F Girard, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1988
Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluidB Gueux, J Fiet, P Couillin, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1989
Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinomaI Henry, S Grandjouan, P Couillin, et al.
Human Genetics|May 1, 1989
Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex regionP Couillin, M Azoulay, I Henry, et al.
Oncogene|December 1, 1988
The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locusT Boehm, I Lavenir, A Forster, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13C Lavedan, F Barichard, M Azoulay, et al.
Genomics|November 1, 1994
A 1.7-Mb YAC contig around the human BDNF gene (11p13): integration of the physical, genetic, and cytogenetic maps in relation to WAGR syndromeM F Rosier, A F Goguel, A Martin, et al.
Genomics|May 15, 1994
Assignment of 112 microsatellite markers to 23 chromosome 11 subregions delineated by somatic hybrids: comparison with the genetic mapP Couillin, E Le Guern, A Vignal, et al.
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