Mutants (48 page)

Dudley, A.T. et al. 2002. A re-examination of proximodistal patterning during vertebrate development.
Nature
418: 539–44

Durham-Pierre, D. et al. 1994. African origin of an intragenic deletion of the human P gene in tyrosine positive oculocutaneous albinism.
Nature Genetics
7: 176–9

Egenvall, A. et al. 2000. Age pattern of mortality in eight breeds of insured dogs in Sweden.
Preventative Veterinary Medicine
46: 1–14

Eigenmann, J.E. 1987. Insulin-like growth factor 1 in dogs.
Frontiers of Hormone Research
17: 161–72

Eigenmann, J.E. et al. 1988. Insulin-like growth factor 1 levels in proportionate dogs, chondrodystrophic dogs and in giant dogs.
Acta Endocrinologica (Copenhagen)
118: 105–8

Eigenmann, J.E. et. al. 1984. Body size parallels insulin-like growth factor 1 levels but not growth hormone secretory capacity.
Acta Endocrinologica (Copenhagen)
106: 448–53

Emery, A.E.H. 1996. Genetic disorders in portraits.
American Journal of Medical Genetics
66: 334–9

Epstein, C.J. et al. 1987. Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in Down syndrome.
Proceedings of the National Academy of Sciences USA
84: 8044–8

Eyre-Walker, A. and P.D. Keightley. 1999. High genomic deleterious mutation rates in hominids.
Nature
397: 334–47

Farrell, H.B. 1984. The two-toed Wadoma – familial ectrodactyly in Zimbabwe.
South African Journal of Medicine
65: 531–3

Fãsseler, P.E. and K. Sander. 1996. Hilde Mangold (1898–1924) and Spemann’s organiser: Achievement and Tragedy.
Wilhelm Roux Archives of Developmental Biology
205: 323–32

Felgenhauer, W.–R. 1969. Hypertrichosis lagnuinosa universalis.
Journal de Génétique humaine
17: 1–44

Ferretti, P. and C. Tickle. 1997. The limbs, in P. Thorogood (ed.)
Embryos, genes and birth defects.
John Wiley and Sons, N.Y.

Figuera, L.E. 1995. Mapping of the congenital generalised hypertrichosis locus to chromosome Xq24-q27. 1.
Nature Genetics
10: 202–6

Finch, C.E. 1990.
Longevity, senescence and the genome.
Chicago University Press

Finch, C.E. and G. Ruvkun. 2001. The genetics of ageing.
Annual Reviews of Genomics and Human Genetics
2: 435–62

Fischer, J.L. 1972. Le concept experimental dans l’oeuvre tératologique d’Etienne Geoffroy Saint-Hilaire.
Revue d’histoire des sciences
25: 347–62

Fischer, J.L. 1991.
Monstres: histoire du corps et de ses défauts.
Syros, Paris

Flanagan, N. et al. 2000. Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation.
Human Molecular Genetics.
9: 2531–7

Flatt, A.E. 1994.
The care of congenital hand anomalies.
Quality Medical Publishing. St Louis. Mo.

Fleischer, R. 1984. Artemis Ephesia. text pp.755–63; plates pp.564–73 in
Lexicon iconographicum mythologiae classicae
II: 1 (text); 2 (plates)

Flurkey, K. et al. 2001. Lifespan extension and delayed immune and collagen aging in mutant mice with defects in growth hormone production.
Proceedings of the National Academy of Sciences USA
98: 6736–41

Forbes, L.S. 1997. The evolutionary biology of spontaneous abortion in humans.
Trends in Ecology and Evolutionary Biology
12: 446–50

Frank, L.G. 1997. Evolution of genital masculinisation: why do female hyenas have such a large ‘penis’?
Trends in Ecology and Evolution
12:58–62

Frankcom, G. and J.H. Musgrave. 1976.
The Irish giant.
Duckworth, UK

Fraser, G. 1877.
Wigtown and Whithorn: historical and descriptive sketches, stories and anecdotes, illustrative of the racy wit and pawky humour of the district.
Gordon Fraser, Wigtown

Fraumeni, J.F 1967. Stature and malignant tumors of bone in childhood and adolesence.
Cancer
20: 967–73

Freire-Maia, A. 1975. Genetics of acheiropodia (the handless and footless families of Brazil). VI. Formal genetic analysis.
American Journal of Human Genetics
27: 521–7

Freire-Maia, A. 1981. Historical note: The extraordinary handless and footless families of Brazil – 50 years of acheiropodia.
American Journal of Human Genetics
9: 31–41

Frey, J. 1994.
Toulouse-Lautrec: a life.
Weidenfeld and Nicolson, London

Frey, J. 1995a. What dwarfed Toulouse-Lautrec?
Nature Genetics
10: 128–30

Frey, J. 1995b. Toulouse-Lautrec’s diagnosis – reply.
Nature Genetics
11: 363

Friedman, J.B. 1981.
The monstrous races in medieval thought and art.
Harvard, Cambridge, Mass.

Fromental-Ramain, C. et al. 1996. Hoxa-13 and Hoxd-13 play a crucial role
in the patterning of the autopod.
Development
122: 2997–3011

Fullerton, S.M. et al. 2000. Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.
American Journal of Human Genetics
67: 881–900

Galis, F. 1999. Why do almost all mammals have seven cervical vertebrae? Developmental constraints, Hox genes, and Cancer.
Journal of Experimental Zoology
285: 19–26

Galis, F. 2001. Why five fingers? Evolutionary constraints on digit number.
Trends in Ecology and Evolution.
16: 637–46

Garcia-Cruz D. et al. 2002. Inherited hypertrichoses.
Clinical Genetics
61: 321–9

Gat, U. et al. 1998. De novo hair follicle morphogenesis and hair tumors in mice expressing a truncated Beta-catenin in skin.
Cell
95: 605–14

Gates, R.R. 1961. The Melanesian dwarf tribe of Aiome, New Guinea.
Acta Geneticae Medicae et Gemellogiae.
10: 277–311

Geffner, M.E. et al. 1995. Insulin-like growth factor 1 resistance in immortalised T cell lines from African Efe pygmies.
Journal of Clinical Endocrinology and Metabolism.
80: 3732–8

Geffner, M.E. et al. 1996. IGF-1 does not mediate T lymphoblast colony formation in response to estradiol, testosterone, 1,25(OH)2, Vitamin D3 and triiodothyronine; studies in control and pygmy lines
Biochemical and Molecular Medicine
59: 72–9

Gegenbauer, C. 1880. Critical remarks on polydactlyly as atavism.
Morphologisches Jahrbuch
6: 584–96

Gehring, W. and K. Ikeo. 1999. Pax 6: mastering eye morphogenesis and eye evolution.
Trends in Genetics
15: 371–7

Geissler, W. et al. 1994. Male pseudohermaphroditism caused by mutations of testicular 17beta-hydroxysteroid dehydrogenase 3.
Nature Genetics
7: 35–9

Gelb, D. et al. 1996. Pycnodysostosis, a lysosomal disease caused by Cathepsin K deficiency.
Science
273: 1236–9

Gelfland, M., C.J. Roberts, and R.S. Roberts. 1974. A two-toed man from the Doma people of the Zambezi Valley.
Rhodesian History
5: 92–5

Geoffroy Saint-Hilaire, E. 1822.
Philosophic anatomique des monstruosités humaines.
Deville-Cavellin, Paris

Geoffroy Saint-Hilaire, E. 1829. Rapport sur le monstre bicéphale Ritta-Christina.
Gazette de Santé
(No. 270)

Geoffroy Saint-Hilaire, E. 1838.
Notions synthétiques, historiques et physi-ologiques de Philosophic Naturelle.
Dénain, Paris

Geoffroy Saint-Hilaire, I. 1832–37.
Histoire générale et particuliére des anomalies de l’organisation chez I’homme et les animaux.
J. B. Balliére, Paris

Geoffroy Saint-Hilaire, I. 1847.
Vie, travaux et doctrine scientifique d’Étienne Geoffroy Saint-Hilaire.
La Société Géologique de France, Paris

Gerhart, J. 2000. Inversion of the chordate body axis: Are their alternatives?
Proceedings of the National Academy of Sciences, USA
97: 4445–8

Gertz, O. 1948. Artemis och hinden frontispisplanschen Linnes Fauna Svecica.
Svenska Linne-Sallskapets Arsskrift
31: 13–37

Gilbert, S.F. 2000.
Developmental biology
(6th edition). Sinauer Associates, Sunderland, Mass.

Glass, B. 1947. Maupertuis and the beginning of genetics.
Quarterly Review of Biology
22: 196–210

Glickman, S.E. et al. 1992. Hormonal correlates of ‘masculinisation’ in female spotted hyenas (
Crocuta crocuta).
1. Infancy to sexual maturity.
Journal of Reproduction and Fertility
95: 451–62

Goding, C.R. 2000. Mitf from neural crest to melanoma: signal transduction and transcription in the melanocyte lineage.
Genes and Development
14: 1712–28

Gong, Y. et al. 1999. Heterozygous mutations in the gene encoding noggin affect human morphogenesis.
Nature Genetics
21: 302–4

Goto, N. et al. 1987. The mexican hairless dog, its morphology and inheritance.
Experimental Animals (Tokyo)
36: 87–90

Goujon, E. 1869. Étude d’un cas d’hermaphrodisme bisexuel imparfait chez l’homme.
Journal de I’anatomie et de la physiologie normales et pathologiques de l’homme et des animaux
6: 599–616

Gould, G.M. and W. L. Pyle. 1897.
Anomalies and curiosities of medicine.
W.B. Saunders, Philadelphia

Gould, S.J. 1981.
The mismeasure of man.
W.W. Norton, N.Y.

Gould, S.J. 1983.
Hen’s teeth and horse’s toes.
W.W. Norton, N.Y.

Graves, J.A. 1998. Interactions between SRY and SOX genes in mammalian sex determination.
Bioessays
20: 264–9

Gravlee, C.G. et al. 2003. Heredity, environment and cranial form: a reanalysis of Boas’s Immigrant data.
American Anthropologist
105: 125–38

Gruber, G.B. 1955. Historisches und aktuelles über das Sirenen-problem in der medizin.
Nova Acta Leopoldina
17: 89–122

Gruman, G.J. 1966. A history of ideas about the prolongation of life.
Transactions of the American Philosophical Society
56: 1–102

Gubbay, J. et al. 1990. A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes.
Nature
346: 245–50

Guichard, C. et al. 2001. Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome).
American Journal of Human Genetics
68: 1030–5

Günther, T. and T. Schinke. 2000. Mouse genetics have uncovered new paradigms in bone biology.
Trends in Metabolism.
11: 189–93

Guyda, H.J. 1998. Growth hormone therapy for non-growth hormone-deficient
children with short stature.
Current Opinion in Pediatrics
10: 416–21

Haldane, J.B.S. 1941.
New paths in genetics.
George Allen & Unwin, London

Hale, F. 1933. Pigs born without eyeballs.
Journal of Heredity
24: 105–6

Haliburton, R.G. 1891.
The dwarfs of Mount Atlas.
David Nutt, London

Haliburton, R.G. 1894. Survivals of dwarf races in the new world.
Proceedings of the American Association for the Advancement of Science
14: 1–14

Hall, B.K. 1995. Atavisms and atavistic mutations.
Nature Genetics
10: 126–7

Hamburger, V. 1947. Monsters in nature.
Ciba Symposia
9: 666–83

Hamburger, V. 1988.
The heritage of experimental embryology: Hans Spemann and the organiser.
Oxford University Press

Hamilton, J.B. 1942. Male hormone stimulation is a prerequisite and an incitant in common baldness.
American Journal of Anatomy
71: 451–80

Hanihara, T. 2000. Frontal and facial flatness of major human populations.
American Journal of Physical Anthropology
111: 105–34

Haraguchi, R. et al. 2000. Molecular analysis of external genitalia formation: the role of fibroblast growth factor (FGF) genes during genital tubercle formation.
Development
127: 2471–9

Harding, R.M. et al. 2000. Evidence for variable selective pressure at MC1R.
American Journal of Human Genetics 66:
1351–61

Hardy, M.H. 1992. The secret life of the hair follicle.
Trends in Genetics
8: 55–61

Harrison, R.G. 1924. Some unexpected results of the heteroplastic transplantation of limbs.
Proceedings of the National Academy of Sciences, USA
10: 69–74

Harvey, R.G. and D.R. Brothwell. 1969. Biosocial aspects of Ainu hirsuteness.
Journal of Biological Sciences
1: 109–24

Harvey, W. 1965.
The works of William Harvey.
Willis, R. (ed., trans.) Sydenham Society, London

Haupt, H. et al. 1990.
he bestiaire de Rodolphe II.
(trans. L. Marcou) Citadelles, Paris

Hayashizaki, Y. ef al. 1989. Thyroid-stimulating hormone (TSH) deficiency caused by a single base substitution in the CAGYC region of the ?-subunit.
EMBO Journal
8: 2291–6

Headon, D.J. and P.A. Overbeek. 1999. Involvement of a novel Tnf receptor homologue in hair follicle induction.
Nature Genetics
22: 370–4

Healy, E. et al. 2001. Functional variation of MC1R alleles from red-haired individuals.
Human Molecular Genetics.
10: 2397–2402

Heijmans, B.T. et al. 2000. Common gene variants, mortality and extreme longevity in humans.
Experimental Gerontology
35: 865–77

Hennessy, R.J. and C.B. Stringer. 2002. Geometric morphometric study of the regional variation of modern human craniofacial form.
American Journal of Physical Anthropology
117: 37–48

Herdt, G. 1994. Mistaken sex: culture, biology and the third sex in New Guinea. in G. Herdt (ed.)
Third sex, third gender.
Zone Books. Cambridge, Mass.

Heron, T.M. 1986.
Boruwlaski, the little count.
Durham, UK

Hertel, C. 2001. Hairy issues: Portraits of Petrus Gonsalus and his family in Archduke Ferdinand IPs
Kunstkammer
and their contexts.
Journal of the History of Collections
13: 1–22