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S.O.S. - BiblioFile
Prime references
A collection of nearly 30,000 prime reprints
3411. Ranke,MB; Pfluger,H; Rosendahl,W; Stubbe,P; Enders,H; Bierich,JR; Majewski,F (1893): Turner Syndrome Spontaneous growth in 150 cases and review of the literature. Eur. J. Pediatr. 141, 81-88.
12524. Funke,O (1902): Pterygium colli. Dtsch. Z. Chir. 63, 162-167.
52770. Rössle,R; Wallart,J (1930): Der angeborene mangel der eierstöcke seine grundsätzliche bedeutung für die theorie der geschlechtsbestimmung. Beitr. Pathol. Anat. Allge. Pathol. 84, 401-452.
10256. Browne,D (1937): The pathology of congenital rings. Arch. Dis. Child. 32, 517.
17622. Turner,HH (1938): A syndrome of infantilism, congenital webbed
neck, and cubitus valgus. Endocrinology 23, 566-574.
<<original report>>
1337. Albright,F; Smith,PH; Fraser,R (1942): A syndrome characterized by primary ovarian insufficiency and decreased stature: Report of 11 cases with a digression on hormonal control of axillary and pubic hair. Am. J. Med. Sci. 204(5/November), 625-648.
7866. Varney,RF; Kenyon,AT; Koch,FC (1942): An association of short stature, retarded sexual development and high urinary gonadotropin titers in women. Ovarian dwarfism. J. Clin. Endoc. 2(3), 137-145.
17502. Moehlig,RC (1942): Intersexuality associated with malignant intra-abdominal teratoma of the seminoma type. Clin. Endocrinol. 2, 257-261.
7822. Wilkins,L; Fleischmann,W (1944): Ovarian agenesis. Patholoy, associated
clinical symptons and the bearing on the theories of sex differentiation.
J. Clin. Endoc. 4(8), 357-375.
<<seminal>>
17612. Castillo,EB del; Balze,FA de la; Argonz,J (1947): Syndrome of
rudimentary ovaries with estrogenic insufficiency and increase in gonadotropins.
Clin. Endocrinol. 7(6), 385-422.
(rest deleted up to: 10 most recent citations)
12486. Kenneson,A; Cramer,DW; Warren,ST (1997): Fragile X Premutations are not a major cause of early menopause. Am. J. Hum. Genet. 61, 1362-1369.
13097. De Schepper,J; Otten,BJ; Francois,I; Bourguignon,J-P; Craen,M; Van der Burgt,I; Massa,GG (1997): Growth hormone therapy in pre-pubertal children with Noonan syndrome: first year growth response and comparison with Turner syndrome. Acta Paediatr. 68, 943-946.
15775. Patsalis,PC; Hadjimarcou,MI; Velissariou,V; Kitsiou-Tzeli,S; Zera,C; Syrrou,M; Lyberatou,E; Tsezou,A; Galla,A; Skordis,N (1997): Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome. Clin. Genet. 51, 184-190.
16072. de Vries,BBA; van den Ouweland,AMW; Mohkamsing,S; Duivenvoorden,HJ; Mol,E; Gelsema,K; van Rijn,M; Halley,RJJ; Sandkuijl,LA; Oostra,BA; Tibben,A; Niermeijer,MF (1997): Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Am. J. Hum. Genet. 61, 660-667.
21761. Patsalis,PC; Hadjimarcou,MI; Velissariou,SV; Kitsiou-Tzeli,CZ; Syrrou,M; Lyberatou,E; Tsezou,AGA; Skordis,N (1997): Supernumerary Marker Chromosomes (SMCs) in Turner Syndrome are Mostly Derived from the Y Chromosome. Clin. Genet. 51, 184-190.
15935. Costa,T; Lambert,M; Teshima,I; Ray,PN; Richer,C-L; Dallaire,L (1998): Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex. Am. J. Med. Genet. 75, 40-44.
15946. Magee,AC; Nevin,NC; Armstrong,MJ; McGibbon,D; Nevin,J (1998): Ullrich-turner syndrome: seven pregnancies in an apparent 45,X woman. Am. J. Med. Genet. 75, 1-3.
22008. Puck,JM; Huntington,FW (1998): X Inactivation in females with
X-linked disease. N. Engl. J. Med. 338(5), 325-328.
<<X chromosome inactivatons non-random>>