Congenital abnormalities in infancy / edited by A.P. Norman.

Date:
1963
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Licence: Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)

Credit: Congenital abnormalities in infancy / edited by A.P. Norman. Source: Wellcome Collection.

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    374 CONGENITAL ABNORMALITIES Langdon-Down J. (1866) Ethnic classification of idiots. Clinical Lectures and Reports, London Hospital 3, 259 Laurence J. Z. & Moon R. C. (1866) Four cases of 'retinitis pigmentosa' occurring in the same family, and accompanied by general imperfections of development. Ophthal. Rev. 2, 32 Lejeune J., Gauthier M. & Turpin R. (1959) Les chromosomes humains en culture de tissus. C.R. Acad. Sci. Paris 248, 602 Lenz W. (1961) Kindliche Misbildungen nach Medikamenteinnahme während der Gravidität? Dtsch. med. Wschr. 86, 2555 Liebman S. D. (1956) Ocular manifestations of Riley-Day syndrome, familial autonomic dysfunction. Arch. Ophthal. 56, 719 Liu M. C. & Corlett K. (1959) A study of congenital heart defects in mongolism. Arch. Dis. Childh. 34, 410 Lowe C. U., Terrey M. & MacLachlan E. A. (1952) Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation. Amer. J. Dis. Child. 83, 164 McCance R. a., Matheson W. J., Gresham G. a. & Elkington I. R. (1960) The cerebro-ocular-renal dystrophies : a new variant. Arch. Dis. Childh. 35, 240 McKenzie J. (1958) Aetiology and treatment of congenital deaf mutism. Brit. Med. J. 2, 201 McKenzie J. & Craig J. (1955) Mandibulo-facial dysostosis (Treacher Collins syndrome). Arch. Dis. Childh. 30, 391 Nager F. R. & de Reynier J. P. (1948) Dyscephalies associated with involvement of ears. Practica Otorhinolaryngol. 10, supp. 2 Norman R. M. (1958) Chapter 5 in Neuropathology by J. G. Greenfield et al. London: Arnold Park E. A. & Powers G. F. (1920) Acrocephaly and scaphocephaly with sym¬ metrically distributed malformations of the extremities : a study of the so-called 'acrocephalosyndactylism'. Amer. J. Dis. Child. 20, 235 Parrot J. (1878) Sur le malformation echondroplastique et le Dieu Phtak. Bull Soc. Anthrop. Paris 1 (N.S.) 296 Patau K., Smith D. W., Therman E., Inhorn S. L. & Wagner H.P. (1960) Multiple congenital anomaly caused by an extra autosome. Lancet 1, 790 Pendred V. (1896) Deaf mutism and goitre. Lancet 2, 532 Penrose L. S. (1961) Mongolism. Clinical Aspects of Genetics, p, 88. London: Pitman's PoLANi P. E. (1961) Turner's syndrome and allied conditions. Brit. Med. Bull. 17, 200 Potter E. L. (1946) Bilateral renal agenesis. J. Pediat. 29, 68 Potter E. L. (1952) Pathology of the Fetus and the Newborn. Chicago: Yr. Bk. Pub. Reinhold J. D. L., Neumark E., Lightwood R. & Carter C. O. (1952) Familial hypoplastic anaemia with congenital abnormalities (Fanconi's syndrome). Blood 7, 915 Richards R. N. (1953) The Möbius syndrome. J. Bone Jt. Surg. 35A, 437 Riley C. M., Day R. L., Greeley D. McL. & Langford W. S. (1949) Central autonomic dysfunction with defective lacrimation. Pediatrics 3, 468 Riley C. M., Freedman A. М. & Langford W. S. (1954) Further observations on familial dysautonomia. Pediatrics 14, 475 Robin E. D. & Gardner F. H. (1957) Hereditary factors in chronic Bright's disease — a study of two affected kindreds. Trans. Ass. Amer. Phys. 70, 140 Robin P. (1934) Glossoptosis due to atresia and hypotrophy of the mandible. Amer. J. Dis. Child. 48, 541