21932595

Source:http://linkedlifedata.com/resource/pubmed/id/21932595

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0005615, umls-concept:C0008059, umls-concept:C0014130, umls-concept:C0086142, umls-concept:C0392760, umls-concept:C1708528
pubmed:issue	7-8
pubmed:dateCreated	2011-9-21
pubmed:abstractText	To develop a reliable and accurate preimplantation genetic diagnosis (PGD) method in six families with endocrine diseases: persistent hyperinsulinemic hypoglycemia of infancy (PHHI), congenital adrenal hyperplasia (CAH) salt-wasting form, Sanjat-Sakati syndrome and multiple endocrine neoplasia 2A (MEN 2A).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9508900
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers
pubmed:status	MEDLINE
pubmed:issn	0334-018X
pubmed:author	pubmed-author:AltarescuGheonaG, pubmed-author:BarenholzOritO, pubmed-author:BeeriRachelR, pubmed-author:BrooksBaruchB, pubmed-author:Eldar-GevaTaliaT, pubmed-author:Levy-LahadEphratE, pubmed-author:MargaliothEhud JEJ, pubmed-author:RenbaumPaulP, pubmed-author:VarshaverIritI
pubmed:issnType	Print
pubmed:volume	24
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	543-8
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:21932595-Abnormalities, Multiple, pubmed-meshheading:21932595-Adrenal Hyperplasia, Congenital, pubmed-meshheading:21932595-Adult, pubmed-meshheading:21932595-Bone Diseases, Developmental, pubmed-meshheading:21932595-Embryo Transfer, pubmed-meshheading:21932595-Endocrine System Diseases, pubmed-meshheading:21932595-Family Health, pubmed-meshheading:21932595-Female, pubmed-meshheading:21932595-Genetic Markers, pubmed-meshheading:21932595-Growth Disorders, pubmed-meshheading:21932595-Humans, pubmed-meshheading:21932595-Hypoparathyroidism, pubmed-meshheading:21932595-Intellectual Disability, pubmed-meshheading:21932595-Israel, pubmed-meshheading:21932595-Male, pubmed-meshheading:21932595-Multiple Endocrine Neoplasia Type 2a, pubmed-meshheading:21932595-Nesidioblastosis, pubmed-meshheading:21932595-Osteochondrodysplasias, pubmed-meshheading:21932595-Pancreatic Diseases, pubmed-meshheading:21932595-Pregnancy, pubmed-meshheading:21932595-Pregnancy Outcome, pubmed-meshheading:21932595-Preimplantation Diagnosis, pubmed-meshheading:21932595-Seizures
pubmed:year	2011
pubmed:articleTitle	Preimplantation genetic diagnosis (PGD)--prevention of the birth of children affected with endocrine diseases.
pubmed:affiliation	Preimplantation Genetic Unit, Zohar PGD Lab, Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel. gheona@szmc.org.il
pubmed:publicationType	Journal Article