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kw.\*:("Sexual differentiation anomaly")

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Ambiguous genitalia : An Indian perspective : Symposium : Endocrinology - Part IIGUPTA, D. K; MENON, P. S. N.Indian journal of pediatrics. 1997, Vol 64, Num 2, pp 189-194, issn 0019-5456Article

Déterminisme et différenciation sexuels chez l'homme : de la pathologie aux gènes = Sex determism and differenciation in man: from phenotype to genotypeVEITIA, R; NUNES, M; MCELREAVEY, K et al.Archives de pédiatrie (Paris). 1997, Vol 4, pp 118s-120s, issn 0929-693X, SUP2Conference Paper

Two SRY-negative XX male brothers without genital ambiguityZENTENO, J. C; LOPEZ, M; VERA, C et al.Human genetics. 1997, Vol 100, Num 5-6, pp 606-610, issn 0340-6717Article

Molecular analysis of the androgen-receptor gene in a family with receptor-positive partial androgen insensitivity : An unusual type of intronic mutationBRÜGGENWIRTH, H. T; BOEHMER, A. L. M; RAMNARAIN, S et al.American journal of human genetics. 1997, Vol 61, Num 5, pp 1067-1077, issn 0002-9297Article

A novel double nucleotide substitution in the HMG box of the SRY gene associated with Swyer syndromeBATTILORO, E; ANGELETTI, B; TOZZI, M. C et al.Human genetics. 1997, Vol 100, Num 5-6, pp 585-587, issn 0340-6717Article

A baboon (Papio hamadryas)with an isochromosome for the long arm of the XMOORE, C. M; LELAND, M. M; BRZYSKI, R. G et al.Cytogenetics and cell genetics. 1998, Vol 82, Num 1-2, pp 80-82, issn 0301-0171Conference Paper

Androgen insensitivity syndrome : A survey of diagnostic procedures and management in the UKVINER, R. M; TEOH, Y; WILLIAMS, D. M et al.Archives of disease in childhood. 1997, Vol 77, Num 4, pp 305-309, issn 0003-9888Article

X chromosome inactivation and micronuclei in normal and Turner individualsHANDO, J. C; TUCKER, J. D; DAVENPORT, M et al.Human genetics. 1997, Vol 100, Num 5-6, pp 624-628, issn 0340-6717Article

PCR-based detection of mosaicism in Turner syndrome patientsYORIFUJI, T; MUROI, J; KAWAI, M et al.Human genetics. 1997, Vol 99, Num 1, pp 62-65, issn 0340-6717Article

Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 geneION, R; TELVI, L; CHAUSSAIN, J.-L et al.Human genetics. 1998, Vol 102, Num 2, pp 151-156, issn 0340-6717Article

Fluorescence in situ hybridization of psu dic(X)(Xpter-Xq21::Xq21-Xpter) in two patients with Turner's syndromeFERNANDEZ, R; PASARO, E.Human heredity. 1998, Vol 48, Num 2, pp 82-86, issn 0001-5652Article

Germ-line and somatic mosaicism in the androgen insensitivity syndrome : Implications for genetic counselingBOEHMER, A. L. M; BRINKMANN, A. O; NIERMEIJER, M. F et al.American journal of human genetics. 1997, Vol 60, Num 4, pp 1003-1006, issn 0002-9297Article

RB1 deletion in gonadoblastoma in an XY femaleANTONINI, S; BARBOSA, A. S; ROSENBERG, C et al.Human genetics. 1997, Vol 101, Num 2, pp 181-185, issn 0340-6717Article

A study of females with deletions of the short arm of the X chromosomeJAMES, R. S; COPPIN, B; DALTON, P et al.Human genetics. 1998, Vol 102, Num 5, pp 507-516, issn 0340-6717Article

Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutationsSCHERER, G; HELD, M; ERDEL, M et al.Cytogenetics and cell genetics. 1998, Vol 80, Num 1-4, pp 188-192, issn 0301-0171Article

Zimmer phocomelia : Delineation by principal coordinate analysisKOSAKI, K; JONES, M. C; STAYBOLDT, C et al.American journal of medical genetics. 1996, Vol 66, Num 1, pp 55-59, issn 0148-7299Article

The genetic and functional basis of isolated 17,20-lyase deficiencyGELLER, D. H; AUCHUS, R. J; MENDONCA, B. B et al.Nature genetics. 1997, Vol 17, Num 2, pp 201-205, issn 1061-4036Article

Donor splice-site mutations in WT1 are responsible for Frasier syndromeBARBAUX, S; NIAUDET, P; MCELREAVEY, K et al.Nature genetics. 1997, Vol 17, Num 4, pp 467-470, issn 1061-4036Article

X-linked sex-reversing genesWACHTEL, S. S.Cytogenetics and cell genetics. 1998, Vol 80, Num 1-4, pp 222-225, issn 0301-0171Article

Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY femalesSCHIEBEL, K; WINKELMANN, M; MERTZ, A et al.Human molecular genetics (Print). 1997, Vol 6, Num 11, pp 1985-1989, issn 0964-6906Article

Posterior hypospadias : long-term followup after reconstructive surgery in the male direction. CommentaryEBERLE, J; ÜBERREITER, S; RADMAYR, C et al.The Journal of urology. 1993, Vol 150, Num 5, pp 1474-1477, issn 0022-5347, 1Article

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