Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1993-8-10
pubmed:abstractText
We describe here a fetus with holoprosencephaly and signs of caudal deficiency sequence. Chromosome examination showed a de novo balanced reciprocal translocation (7;22) (q36;q11) with loss of the derivative chromosome 22 in 50% of the cells examined. The present report and available published data indicate that the terminal region of the long arm of chromosome 7 contains genes implicated in the development of the central nervous system and the caudal region.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-1897576, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-2045103, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-2241084, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-2309771, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-2624261, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-2805383, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-3087168, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-3119853, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-3189331, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-3605204, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-3706408, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-511152, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-6199974, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-6430085, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-6758992, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-6831934, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-6859113, http://linkedlifedata.com/resource/pubmed/commentcorrection/8326499-912940
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0022-2593
pubmed:author
pubmed:issnType
Print
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
521-4
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1993
pubmed:articleTitle
Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter.
pubmed:affiliation
Service d'Histologie, Embryologie et de Cytogénétique, Hôpital Necker-Enfants, Malades, Paris, France.
pubmed:publicationType
Journal Article, Review, Case Reports