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The British Journal of Dermatology|September 1, 1995
Keratoderma with scleroatrophy of the extremities or sclerotylosis (Huriez syndrome): a reappraisalE Delaporte, C N'guyen-Mailfer, A Janin, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1988
Congenital acute monoblastic leukemia with double translocation (8;16) (p11;p13) and (16;20) (q13;p13)M Zandecki, J L Laï, F Mazingue, et al.
Cancer Genetics and Cytogenetics|May 1, 1989
Translocation t(10;17)(p13;q12) in two cases of acute nonlymphocytic leukemia with phagocytic activity of blasts. A new cytogenetic entity?J L Laï, M H Estienne, P Fenaux, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1997
[Prenatal diagnosis of partial trisomy 9p]S Vanderstichele, J B Savary, P Dufour, et al.
Acta Dermato-Venereologica|May 6, 1999
Excision repair defect in Rothmund Thomson syndromeF Vasseur, E Delaporte, M T Zabot, et al.
Blood|September 1, 1988
Cytogenetic studies and their prognostic significance in agnogenic myeloid metaplasia: a report on 47 casesJ L Demory, B Dupriez, P Fenaux, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1993
[Partial 12q trisomy and chylothorax]V Houfflin, P Dufour, D Vinatier, et al.
Presse Medicale (Paris, France : 1983)|January 9, 2001
[Trisomy 18: ultrasound aspects. Report of 40 cases]L Brun, P Dufour, J B Savary, et al.
Cancer Genetics and Cytogenetics|September 1, 1990
Chronic myeloid leukemia with unusual variant Ph translocation (22;22)(q11;q13). Two cases with chimeric BCR-ABL transcriptsJ L Laï, Z Aissaoui, C Collyn-d'Hooghe, et al.
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