Literature DB >> 5303427

[The Dr phenotype: a study of threee cases with a ring D chromosome].

J Lejeune, J Lafourcade, R Berger, J Cruveiller, M O Rethoré, B Dutrillaux, D Abonyi, H Jérôme.   

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Year:  1968        PMID: 5303427

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


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  25 in total

1.  Derivative chromosomal structures from a ring chromsome 4.

Authors:  R Niss; E Passarge
Journal:  Humangenetik       Date:  1975-05-26

Review 2.  Malformations of kidney and urinary tract in common chromosomal aberrations. II. Morphogenetic studies.

Authors:  G Töndury
Journal:  Humangenetik       Date:  1973-03-23

3.  The phenomenon of premature chromosome condensation: its relevance to basic and applied research.

Authors:  K Sperling; P N Rao
Journal:  Humangenetik       Date:  1974

4.  Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.

Authors:  R J Warren; D L Rimoin; R L Summitt
Journal:  Am J Hum Genet       Date:  1973-01       Impact factor: 11.025

5.  [Ocular manifestations in diseases caused by aberrations in non-sexual chromosomes].

Authors:  H Saraux
Journal:  J Med Genet       Date:  1970-09       Impact factor: 6.318

Review 6.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

7.  Ring 13 chromosome with normal haptoglobin inheritance.

Authors:  J G Hollowell; L G Littlefield; A Dharmkrong-AT; G M Folger; C W Heath; G E Bloom
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

8.  The 13q- deletion syndrome.

Authors:  E Grace; J Drennan; D Colver; R R Gordon
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

9.  The aetiology of the cat eye syndrome reconsidered.

Authors:  G Guanti
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

Review 10.  Constitutional ring chromosomes and tumour suppressor genes.

Authors:  N Tommerup; R Lothe
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

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