Treasury of human inheritance Volume 1 [...] Name and subject indices to volume 1 / by Julia Bell, M.A.

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Bibliographische Detailangaben
1. Verfasser: Bell, Julia (VerfasserIn)
Körperschaft: Francis Galton Laboratory for National Eugenics (Herausgebendes Organ)
Weitere Verfasser: Fisher, Ronald Aylmer (HerausgeberIn), Pearson, Karl (HerausgeberIn)
Format: UnknownFormat
Sprache:eng
Veröffentlicht: Cambridge University Press 1912
Schriftenreihe:Eugenics laboratory memoirs 16
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Titel Jahr Band
Treasury of human inheritance Volume 5 On hereditary digital anomalies Part 3 The @Laurence-Moon syndrome / by Julia Bell, M.A., F.R.C.P. 1958
Treasury of human inheritance Volume 5 On hereditary digital anomalies Part 2 On syndactyly and its association with polydactyly / by Julia Bell, M.A., F.R.C.P. ; with a note by L. S. Penrose, M.A., M.D. 1953
Treasury of human inheritance Volume 4 Nervous diseases and muscular dystrophies Part 2 On the peroneal type of progressive muscular athrophy / by Julia Bell, M.A., M.R.C.P. (Under the Medical Research Council) 1935
Treasury of human inheritance Volume 4 Nervous diseases and muscular dystrophies Part 1 Huntington's Chorea / by Julia Bell, M.A., M.R.C.P. (Under the Medical Research Council) 1934
Treasury of human inheritance Volume 2 Anomalies and diseases of the eye : Nettleship memorial volume Part 4 Hereditary optic atrophy (Leber's disease) / by Julia Bell, M.A., M.R.C.P. 1931
Treasury of human inheritance Volume 2 Anomalies and diseases of the eye : Nettleship memorial volume Part 3 Blue Sclerotics and fragility of bone / by Julia Bell, M.A., M.R.C.P. 1928
Treasury of human inheritance Volume 2 Anomalies and diseases of the eye : Nettleship memorial volume Part 2 Colour-blindness / by Julia Bell, M.A., M.R.C.S., L.R.C.P. 1926
Treasury of human inheritance Volume 3 Hereditary disorders of bone development Part 1 Diaphysial aclasis (multiple exostoses), multiple enchondromata, cleido-cranial dystosis / by Percy Stocks, M.D., D.P.H. with the assistance of Amy Barrington 1925
Treasury of human inheritance Volume 2 Anomalies and diseases of the eye : Nettleship memorial volume Part 1 Retinitis pigmentosa and allied diseases congenital stationary night-blindness Glioma retinae / by Julia Bell, M.A., M.R.C.S., L.R.C.P. ; with a memoir of Edward Nettleship by J.B. Lawford, LL.D., F.R.C.S. 1922
Treasury of human inheritance Volume 1 Part 7/8 Dwarfism / by H. Rischbieth, M.A., MD. Cantab., F.R.C.S. Eng. and Amy Barrington, Eugenics Laboratory 1912
Treasury of human inheritance Volume 1 [...] Name and subject indices to volume 1 / by Julia Bell, M.A. 1912
Treasury of human inheritance Volume 1 Part 5/6 Haemophilia / by William Bulloch, M.D. and Paul Fildes, M.B. B.C. 1911
Treasury of human inheritance Volume 1 Part 4 Hare-lip and cleft palate / by H. Rischbieth, M.A., M.D., B.C. (Cantab.), F.R.C.S. Eng 1910
Treasury of human inheritance Volume 1 Part 1/2 1909
Treasury of human inheritance Volume 1 Part 3 1909
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