Literature DB >> 14148996

KINDRED SHOWING CONGENITAL ABSENCE OF THE DERMAL RIDGES (FINGERPRINTS) AND ASSOCIATED ANOMALIES.

H W BAIRD.   

Abstract

Entities:  

Keywords:  ABNORMALITIES; BLOOD GROUPS; CHILD; CONTRACTURE; DERMATOGLYPHICS; ECTODERMAL DEFECT, CONGENITAL; FINGERS; GENETICS, HUMAN; INFANT, NEWBORN; SWEATING; TOES

Mesh：

Substances：

Year:  1964        PMID： 14148996     DOI： 10.1016/s0022-3476(64)80610-7

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  12 in total

1.  Dental defects associated with neonatal symptomatic hypocalcaemia.

Authors:  L Stimmler; G J Snodgrass; E Jaffe
Journal:  Arch Dis Child       Date:  1973-03       Impact factor: 3.791

2.  Congenital malformations of human dermatoglyphs.

Authors:  T J David
Journal:  Arch Dis Child       Date:  1973-03       Impact factor: 3.791

3.  Camptodactyly: occurrence in two new genetic syndromes and its relationship to other syndromes.

Authors:  R M Goodman; M B Katznelson; E Manor
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

4.  [Dysplasia of epidermal ridges with autosomal dominant transmission. Dermatoglyphic studies of one family].

Authors:  P Dodinval; P Leblanc; C Delree; P Deslypere
Journal:  Humangenetik       Date:  1971

5.  Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance.

Authors:  H Gordon; D Davies; M Berman
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

6.  Brachydactyly and polydactyly with dermal ridge dissociation and ridge hypoplasia.

Authors:  M D Crawfurd; P Saldaña-Garcia
Journal:  J Med Genet       Date:  1979-10       Impact factor: 6.318

7.  Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14.

Authors:  Jennie Lugassy; Peter Itin; Akemi Ishida-Yamamoto; Kristen Holland; Susan Huson; Dan Geiger; Hans Christian Hennies; Margarita Indelman; Dani Bercovich; Jouni Uitto; Reuven Bergman; John A McGrath; Gabriele Richard; Eli Sprecher
Journal:  Am J Hum Genet       Date:  2006-08-25       Impact factor: 11.025

8.  Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome.

Authors:  Ming Li; Jianbo Wang; Zhenlu Li; Jia Zhang; Cheng Ni; Ruhong Cheng; Zhirong Yao
Journal:  Eur J Hum Genet       Date:  2016-03-02       Impact factor: 4.246

9.  [Dysplasia of epidermal ridges. Evidence of an apical dysplasia of the fingers].

Authors:  P Dodinval
Journal:  Humangenetik       Date:  1972

10.  Naegeli-Franceschetti-Jadassohn syndrome: A rare case.

Authors:  Bela J Shah; Ashish K Jagati; Neha P Gupta; Suyog S Dhamale
Journal:  Indian Dermatol Online J       Date:  2015 Nov-Dec
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