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| - wetenschappelijk artikel (nl)
- article scientifique publié en 1980 (fr)
- наукова стаття, опублікована в лютому 1980 (uk)
- im Februar 1980 veröffentlichter wissenschaftlicher Artikel (de)
- artículu científicu espublizáu en febreru de 1980 (ast)
- scientific article published on 01 February 1980 (en)
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| - The chromosomal basis of human infertility
- Chromosomal evolution in Primates: Tentative phylogeny from Microcebus murinus (Prosimian) to man
- A new technic of analysis of the human karyotype
- Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7
- Trisomy 18qter and trisomy mapping of chromosome 18
- A cytogenetic survey of 11,680 newborn infants
- A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities
- Systematic analysis of 95 reciprocal translocations of autosomes
- Incidence and mutation rates of structural rearrangements of the autosomes in man.
- Chromosome anomalies among livebirths
- Cytogenetics of Recurrent Abortions
- Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10),rec(10), in her son
- Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18
- A closer look at chromosomal inversions
- Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers
- Abnormalities resulting from a familial pericentric inversion of chromosome 18
- Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18
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| - Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (en)
- Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (nl)
- Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (sq)
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| skos:prefLabel
| - Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (en)
- Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (nl)
- Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (sq)
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| name
| - Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (en)
- Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (nl)
- Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (sq)
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| title
| - Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling (en)
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