Literature DB >> 4249677

Dermatoglyphic nomogram for the diagnosis of Down's syndrome.

T E Reed, D S Borgaonkar, P M Conneally, P Yu, W E Nance, J C Christian.   

Abstract

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Year:  1970        PMID： 4249677     DOI： 10.1016/s0022-3476(70)80087-7

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


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  9 in total

1.  Diagnosis of Down's syndrome at birth.

Authors: 
Journal:  Br Med J       Date:  1976-10-09

2.  Double autosomal trisomy and mosaicism for chromosomes no. 8 and no. 21.

Authors:  M G Wilson; A Fujimoto; O S Alfi
Journal:  J Med Genet       Date:  1974-03       Impact factor: 6.318

3.  Dermatoglyphic heterogeneity in mongolis with congenital heart disease.

Authors:  T Reed; L Shields; W E Nance
Journal:  Am J Hum Genet       Date:  1973-01       Impact factor: 11.025

4.  Apparent G-monosomy, G-deletion, and incomplete Down's syndrome in a single family.

Authors:  R Schmidt; G Mundel; M Rosenblatt; M B Katznelson
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

5.  Two Robertsonian translocations in a boy with mental retardation.

Authors:  E Lieber; P Shah
Journal:  J Med Genet       Date:  1982-06       Impact factor: 6.318

6.  Dic(21;21) in a Down's syndrome child with an unusual chromosome 9 variant in the mother.

Authors:  J M Berg; H A Gardner; R J Gardner; E G Goh; V D Markovic; N E Simpson; R G Worton
Journal:  J Med Genet       Date:  1980-04       Impact factor: 6.318

7.  Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.

Authors:  J D Williams; R L Summitt; P R Martens; R A Kimbrell
Journal:  Am J Hum Genet       Date:  1975-07       Impact factor: 11.025

8.  Dermatoglyphic study in children with phenylketonuria.

Authors:  S Balci; F Tanzer; M Atasu; I Ozalp
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

9.  Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation.

Authors:  K Taysi; R S Sparkes; T J O'Brien; D R Dengler
Journal:  J Med Genet       Date:  1982-04       Impact factor: 6.318
  9 in total

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