Literature DB >> 393324

Genetic counseling in sex linkage.

N E Morton, J M Lalouel.   

Abstract

Mesh：

Year:  1979        PMID： 393324

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  6 in total

1.  Autosomal dominant anterior polar cataracts associated with a familial 2;14 translocation.

Authors:  T Moross; S S Vaithilingam; S Styles; H A Gardner
Journal:  J Med Genet       Date:  1984-02       Impact factor: 6.318

2.  Genetic counselling in haemophilia by discriminant analysis 1975-1980.

Authors:  E S Barrow; C H Miller; H M Reisner; J B Graham
Journal:  J Med Genet       Date:  1982-02       Impact factor: 6.318

3.  Transition matrices with mutation.

Authors:  N E Morton; N Yasuda
Journal:  Am J Hum Genet       Date:  1980-03       Impact factor: 11.025

4.  A probable sex difference in mutation rates in ornithine transcarbamylase deficiency.

Authors:  C Bonaïti-Pellié; A Pelet; H Ogier; J R Nelson; C Largillière; J Berthelot; J M Saudubray; A Munnich
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132

5.  A maximum likelihood estimate of the sex ratio of mutation rates in haemophilia A.

Authors:  R M Winter; E G Tuddenham; E Goldman; K B Matthews
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

6.  Detection of carriers for Duchenne muscular dystrophy. Quality control of creatine kinase assay.

Authors:  H Plauchu; C Junien; I Maire; R Said; R Gozlan; J M Lalouel
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132
  6 in total

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