Literature DB >> 6655679

A father and daughter with fragile X chromosome.

S Morić-Petrović, Z Laća.   

Abstract

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Year:  1983        PMID： 6655679      PMCID： PMC1049190     

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  1 in total

1.  Inherited congenital normofunctional testicular hyperplasia and mental deficiency. A corroborative study.

Authors:  J M Cantú; H E Scaglia; M González-Diddi; P Hernández-Jáuregui; T Morato; M E Moreno; J Giner; A Alcántar; D Herrera; G Pérez-Palacios
Journal:  Hum Genet       Date:  1978-04-24       Impact factor: 4.132
  1 in total
  2 in total

1.  FMR1 CGG-repeat instability in single sperm and lymphocytes of fragile-X premutation males.

Authors:  S L Nolin; G E Houck; A D Gargano; H Blumstein; C S Dobkin; W T Brown
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

2.  Apparent regression of the CGG repeat in FMR1 to an allele of normal size.

Authors:  L Vits; K De Boulle; E Reyniers; I Handig; J K Darby; B Oostra; P J Willems
Journal:  Hum Genet       Date:  1994-11       Impact factor: 4.132
  2 in total

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