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www.ncbi.nlm.nih.gov/pmc/articles/PMC1932384/pdf/ajhg00...
www.ncbi.nlm.nih.gov/pmc/articles/PMC1932384/pdf/ajhg00553-0045.pdf
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that there are at least three dominant forms of congenital deaf-mutism. Recently, in a monograph edited by Kallman, Sank (1962) presented pre- liminary data ...
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www.sciencedirect.com/science/article/pii/0002870357900...
www.sciencedirect.com/science/article/pii/0002870357900790
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Four cases of deaf-mutism combined with a peculiar heart disease have been observed in one family. The parents and 2 other children were healthy and had ...
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onlinelibrary.wiley.com/doi/10.1111/j.1755-3768.1950.tb...
onlinelibrary.wiley.com/doi/10.1111/j.1755-3768.1950.tb05362.x/pdf
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CONGENITAL DEAF-MUTISM IN A FAMILY WITH. DYSTROPHIA RETICULARIS LAMINAE PIGMENTOSAE. RETINAE (SJOGREN). By Stig HoEmgien.') ...
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eurheartj.oxfordjournals.org/content/8/5/528.abstract
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A family is presented in which there is a high incidence of hypertrophic cardiomyopathy and congenital deaf-mutism. The two abnormalities occurred together in ...
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eurheartj.oxfordjournals.org/content/8/5/528.full.pdf
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KEY WORDS: Hypertrophic cardiomyopathy, congenital deaf-mutism, enhanced familial incidence, mode of inheritance. A family is presented in which there is a ...
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archderm.ama-assn.org/cgi/reprint/89/1/151.pdf
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Albinism and. Congenital Deaf-Mutism. L. ZIPRKOWSKI, MD. AND. A. ADAM, PhD. TEL HASHOMER, ISRAEL. Simultaneous occurrence of autosomal re- ...
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pointinjection.com/ht/deaf.mutism.shtml
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Sep 27, 2008 ... Congenital deaf-mutism is also a possible etiology. After regaining hearing the next problem is the speech. In such cases the child should be ...
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www.mendeley.com/research/keratoderma-hereditarium-muti...
www.mendeley.com/research/keratoderma-hereditarium-mutilans-vohwinkels-syndrome-associated-congenital-deafmutism/
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(1995) Peris et al. The British journal of dermatology. Keratoderma hereditarium mutilans, or Vohwinkel's syndrome, is a rare cutaneous disorder which is ...
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www.komci.org/GSResult.php?RID=0048KJD%2F2011.49.4.379&...
www.komci.org/GSResult.php?RID=0048KJD%2F2011.49.4.379&DT=6
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Erythrokeratodermia Variabilis with Congenital Deaf-Mutism Nam HM, Kim UK, Park K, Park SD. Korean J Dermatol 2011 Apr 49(4):379-381. Korean.
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