These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
64 related articles for article (PubMed ID: 5514155)
1. A study of dermatoglyphics and the simian crease in familial deafness. Dar H; Winter ST Hum Hered; 1970; 20(5):493-506. PubMed ID: 5514155 [No Abstract] [Full Text] [Related]
2. [Characteristics of the dermatoglyphics of the hand in congenital deaf-mutism]. Gagaeva LF Tsitol Genet; 1977; 11(2):109-13. PubMed ID: 883019 [TBL] [Abstract][Full Text] [Related]
3. Familial hand abnormality and sensori-neural deafness: a new syndrome. Stewart JM; Bergstrom L J Pediatr; 1971 Jan; 78(1):102-10. PubMed ID: 5539065 [No Abstract] [Full Text] [Related]
5. [Achalasia with dolichomegaesophagus associated with perceptual deafness of perception and familial 4:9 balanced translocation]. Pescia G; Jotterand-Bellomo M; Vecerina S; Lanao C Rev Med Suisse Romande; 1981 Apr; 101(4):263-8. PubMed ID: 7256057 [No Abstract] [Full Text] [Related]
6. Some aspects on the dermatoglyphics of normal and defective children in Bulgaria. Tornjova-Randelova SG Anthropol Anz; 1994 Dec; 52(4):351-5. PubMed ID: 7840541 [TBL] [Abstract][Full Text] [Related]
8. Familial nephritis and associated deafness in a southwestern Apache Indian family. Westley CR South Med J; 1970 Dec; 63(12):1415-9. PubMed ID: 5486417 [No Abstract] [Full Text] [Related]
9. Incidence of simian crease in normal Nepalese children. Malla T; Malla KK; Gauchan E; Brijesh S; Sharma R Kathmandu Univ Med J (KUMJ); 2010; 8(32):410-4. PubMed ID: 22610771 [TBL] [Abstract][Full Text] [Related]
10. The Nathalie syndrome. A new hereditary syndrome. Cremers CW; Ter Haar BG; Van Rens TJ Clin Genet; 1975 Nov; 8(5):330-40. PubMed ID: 1204231 [TBL] [Abstract][Full Text] [Related]
11. [Dermatoglyphics and creases in a family with brachydactyly (type Drinkwater I) to the question of the relation between dematoglyphics and four-finger-crease (author's transl)]. Vormittag W; Weninger M; Frisch H Anthropol Anz; 1975 Oct; 35(1):1-6. PubMed ID: 1052862 [TBL] [Abstract][Full Text] [Related]
12. The simian and Sydney crease. Wertelecki W Birth Defects Orig Artic Ser; 1979; 15(6):455-71. PubMed ID: 162224 [No Abstract] [Full Text] [Related]
13. Palmar crease variants and their clinical significance: a study of newborns at risk. Dar H; Schmidt R; Nitowsky HM Pediatr Res; 1977 Feb; 11(2):103-8. PubMed ID: 138837 [TBL] [Abstract][Full Text] [Related]
14. Dermatoglyphics and the simian crease in infants of low birth weight. A pilot study. Dar H; Carney FE; Winter ST Acta Paediatr Scand; 1971 Jul; 60(4):479-81. PubMed ID: 5556390 [No Abstract] [Full Text] [Related]
15. [Associated anterior lenticonus, deafness and familial nephropathy(Alport's syndrome)]. Ardouin M; Coutel Y; Bourguet J; Urvoy M; Thomet G J Genet Hum; 1966; 15():Suppl:44-8. PubMed ID: 4968158 [No Abstract] [Full Text] [Related]
16. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Prezant TR; Agapian JV; Bohlman MC; Bu X; Oztas S; Qiu WQ; Arnos KS; Cortopassi GA; Jaber L; Rotter JI Nat Genet; 1993 Jul; 4(3):289-94. PubMed ID: 7689389 [TBL] [Abstract][Full Text] [Related]