Zobrazeno 1 - 10
of 234
pro vyhledávání: '"Dodinval, P."'
Publikováno v:
Acta Genetica et Statistica Medica, 1964 Jan 01. 14(3/4), 327-337.
Externí odkaz:
https://www.jstor.org/stable/45103650
Autor:
Dodinval, P. A.
Publikováno v:
Human Heredity, 1970 Jan 01. 20(2), 169-177.
Externí odkaz:
https://www.jstor.org/stable/45101888
Autor:
Dodinval, P. A.
Publikováno v:
Human Heredity, 1973 Jan 01. 23(1), 59-68.
Externí odkaz:
https://www.jstor.org/stable/45100983
Autor:
Szpiro-Tapia S, Kaplan J, Anastella PELET, Guilloud-Bataille M, Heuertz S, Nivelon-Chevallier A, Mathieu M, Piussan C, Journel H, Dodinval P
Publikováno v:
Europe PubMed Central
Anhidrotic ectodermal dysplasia is an X-linked inherited skin disorder; only affected males exhibit the complete syndrome, whereas females may have a few mild features. The gene involved in this disease is located in the proximal area of the long arm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ab08d827737db5e2ef2bcbd6c7e6cac6
https://pubmed.ncbi.nlm.nih.gov/2316957
https://pubmed.ncbi.nlm.nih.gov/2316957
Publikováno v:
Clinical Genetics; Mar1989, Vol. 35 Issue 3, p205-208, 4p
Partial trisomy 20q due to paternal t(8;20) translocation: Case report and review of the literature.
Publikováno v:
Clinical Genetics; May1988, Vol. 33 Issue 5, p386-389, 4p
Publikováno v:
Acta Neuropathologica; 1981, Vol. 53 Issue 2, p87-91, 5p
Autor:
Verloes, A., Dodinval, P.
Publikováno v:
Ophthalmic Paediatrics & Genetics; 1990, Vol. 11 Issue 1, p41-47, 7p
Publikováno v:
Prenatal Diagnosis; Feb1991, Vol. 11 Issue 2, p129-132, 4p