Zobrazeno 1 - 3
of 3
pro vyhledávání: '"M. J. Timmerman"'
Publikováno v:
Clinical Genetics. 22:102-104
The present report describes a 46,XX,inv(3)(p13p25) karyotype in a 4.5year-old girl with growth retardation and in her phenotypically normal mother.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02a966cad3e5bb5c5c132cd9489dd91d
https://doi.org/10.1111/j.1399-0004.1982.tb01421.x
https://doi.org/10.1111/j.1399-0004.1982.tb01421.x
Publikováno v:
Clinical genetics. 25(1)
The phenotype of a boy with monosomy of a small segment of chromosome (10) (q24.2----q25.3) is described. In his family a balanced insertion (5;10) is found in three generations. Moreover there are two persons who are trisomic for the same small segm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dd13c2c10a8f03e0bfe6f3d0b6ae34d
https://pubmed.ncbi.nlm.nih.gov/6705241
https://pubmed.ncbi.nlm.nih.gov/6705241