Hypoparathyroidism, retarded growth and development, and dysmorphism or Sanjad-Sakati syndrome: an A...
Hypoparathyroidism, retarded growth and development, and dysmorphism or Sanjad-Sakati syndrome: an Arab disease reminiscent of Kenny-Caffey syndrome
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England: BMJ Publishing Group Ltd
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English
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England: BMJ Publishing Group Ltd
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5 The same authors subsequently suggested that this entity represents the Arab variant of KCS and because of some clinical resemblance to DiGeorge syndrome (DGS) they suggested that the phenotype is the result of 22q11 microdeletion or some abnormality of chromosome 10p where a second locus for DGS lies. 6 This entity was originally described by Sa...
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Full title
Hypoparathyroidism, retarded growth and development, and dysmorphism or Sanjad-Sakati syndrome: an Arab disease reminiscent of Kenny-Caffey syndrome
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1734523
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1734523
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ISSN
0022-2593,1468-6244
E-ISSN
1468-6244
DOI
10.1136/jmg.37.2.145
