Profound Childhood Deafness I5I

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Profound Childhood Deafness
Usher, C. H. (1914). On the inheritance of retinitis pigmentosa,
with notes of cases. Roy. Lond. ophthal. Hosp. Rep., 19, I30.
Van der Hoeve, J. (39I6). Abnorme Lange der Tranenrohrchen
mit Ankyloblepharon. Klin. Mbl. Augenheilk., 56, 232.
- (1923).
Relations between the eye and ear (including the
vesticular organ). Ann. Otol. (St. Louis), 32, 571.
-, and de Kleiin, A.
(I917). Blauwe sclera, broosheid van het
beenstelsel en gehoorstoornissen. Ned. T. Geneesk., 6I (i), 1003.
Van Dishoeck, H. A. E., and Bierman, T. A. (1957). Sudden
perceptive deafness and viral infection (report of the first one
hundred patients). Ann. Otol. (St. Louis), 66, 963.
Laryng.,
Van Egmond, A. A. J. (1954). Congenital deafness.
J.
68, 429.
Van Gilse, P. H. G. (1926). Geval van pigmentanomalie en doofheid. Ned. T. Geneesk., 70 (ii), 479.
Vitello, A. (I939). Una particolare varietk di malattia famigliare:
sordomutismo congenito, retinite pigmentosa ed atassia di Marie.
Pisani, 59. 129.
Voltolini, R. (I882). Die acute Entzindung des hautigen Labyrinthes des Ohres (Otitis labyrinthica s. intima) irrthumlich fur Meningitis cerebro-spinalis epidemica gehalten. Morgenstern, Breslau.
Von Graefe, A. (I858). Vereinzelte Beobachtungen und Bemerkungen. 6. Exceptionelles Verhalten des Gesichtfeldes bei
Pigmententartung der Netzhaut. Albrecht v. Graefes Arch.
Ophthal., 4, Abt 2, 250.
Voss, 0. (1923). Geburtstrauma und Gehororgan. Z. Hals-,
Nas.- u. Ohrenheilk., 6, I82.
Waardenburg, P. J. (I95I). A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with
pigmentary defects of the iris and head hair and with congenital
deafness. Amer. hum. Genet., 3, 195.
(I956). Intermarriages of hereditarily deaf mute and of
hereditarily blind people, marriage counselling and the question
of sterilization. Acta genet. (Basel), 6, I13.
Ward, 0. C. (I964). A new familial cardiac syndrome in children.
Irish med. Ass., 54, 103.
Wardrop, J. (I813). History of James Mitchell, a Boy Born Blind
and Deaf, with an Account of the Operation Performed for the
Recovery of his Sight. Murray, London.
Werner, H. (I932). Geschichte des Taubstummenproblems bis ins
I7 Jahrhundert. Fischer, Jena.
Whetnall, E., and Fry, D. B. (I964). The Deaf Child. Heinemann,
J.
J.
London.
Wibaut, F. (I93 ). Studien uber Retinitis pigmentosa. I. Statistische Grunde fur die Annahme das die Retinitis pigmentosa
in genetischem Sinne keine Einheit darstellt. Klin. Mbl. Augenheilk., 87, 298.
Wilde, W. R. (I853). Practical Observations on Aural Surgery and
the Nature and Diagnosis of Diseases of the Ear. Blanchard and
Lea, Philadelphia; Churchill, London.
I5I
Wildervanck, L. S. (1952). Een geval van aandoening van Klippel-Feil, gecombineerd met abducensparalyse, retractio bulbi
en doofstomheid. Ned. T. Geneesk., 96, 2752.
- (1953).
Heredity and Deafness. Proc. Int. Course Paedoaudiol., Grdningen, p. 39.
(I957a). De etiologie van doofstomheid. Ned. T. Geneesk.,
101,
1347-
(I957b). Doofstomme kinderen met het syndroom
denburg-Klein. ibid., OI, I120.
van
Waar-
(I957c). Audiometric examination of parents of children
deaf from birth. The influence of consanguineous marriage.
Arch. Otolaryng., 65, 280.
Dysostosis mandibulo-facialis (Franceschetti(Ig6oa).
Zwahlen) in four generations. Acta Genet. med. (Roma), 9, 447.
(ig6ob). Een cervico-oculo-acusticussyndroom. Ned. T.
Geneesk., 104, 2600.
(I962). Hereditary malformations of the ear in three generations. Marginal pits, pre-auricular appendages, malformations
of the auricle and conductive deafness. Acta oto-laryng. (Stockh.),
549 553-
(I963). Perceptive deafness associated with split-hand and
-foot, a new syndrome? Acta genet. (Basel), 13, I6I.
Wilhelmi, B. F. (I873). Statistik der Taubstummen des Regierungsbezirkes Magdeburg, nach der Volkszahlung von I871.
Mbl. med. Stat. off. Gesundhpfl. Dtsch. Klin., 25, Suppl. 9, 65.
Williams, F., and Roblee, L. A. (I962). Hereditary nerve deafness.
A follow-up of four cases in one family. Arch. Otolaryng., 75, 69.
Wilson, T. G., and Kane, F. (I959). Congenital deafness in white
cats. Acta oto-laryng. (Stockh.), 50, 269.
Winckel, C. W. F. (I948). Quinine and congenital injuries of
ear and eye of the foetus.
trop. Med. Hyg., 51, 2.
Wolff, D. (1942). Microscopic study of temporal bones in dysostosis multiplex (gargoylism). Laryngoscope (St. Louis), 52, 2I8.
Yearsley, M. (1934). An analysis of over four thousand cases of
educational deafness studied during the past 25 years. Brit.
Child. Dis., 31, I77 and 272.
(1935). An analysis of over four thousand cases of educational
deafness studied during the past 25 years. ibid., 32, 2I, I07, I96,
J.
J.
-
and 264.
Zelig, S. (I96I). Syndrome of Waardenburg with deafness. Laryngoscope (St. Louis), 71, 19.
Ziprkowski, L., and Adam, A. 'I964). Recessive total albinism and
congenital deaf-mutism. Arch. Derm., 89, I51.
-, Krakowski, A., Adam, A., Costeff, H., and Sade, J.
(r962).
Partial albinism and deafmutism due to a recessive sex-linked
gene. ibid., 86, 530.
Zonderman, B. (I959). The preschool nerve-deaf child. Study of
etiological factors. Laryngoscope (St. Lous), 69, 54.
Corrigenda
A Family Apparently Showing Transmission of a Translocation between Chromosome 3 and one of the
'X-6-12' or 'C' Group. G. Clarke, A. C. Stevenson, Pamela Davies, and C. E. Williams. Vol. I, p. 27.
The Table on p. 3I requires the following corrections:
III.7 Substitute MSNs for MsNs
II.5 Substitute MSMs for MNS
,,
,,
II.6
R,r for R2r
MSMs for MMs
III.7
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Corrigenda
J Med Genet 1964 1: 151
doi: 10.1136/jmg.1.2.151
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