| Attributes | Values |
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| rdf:type
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| description
| - videnskabelig artikel (da)
- article científic (ca)
- article scientific (oc)
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- articolo scientifico (it)
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- artigo científico (pt)
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- artikull shkencor (sq)
- artikulong pang-agham (tl)
- artykuł naukowy (pl)
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- bilimsel makale (tr)
- scienca artikolo (eo)
- teaduslik artikkel (et)
- tieteellinen artikkeli (fi)
- tudományos cikk (hu)
- vedecký článok (sk)
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- vitenskapelig artikkel (nb)
- vitskapeleg artikkel (nn)
- vědecký článek (cs)
- wetenschappelijk artikel (nl)
- wissenschaftlicher Artikel (de)
- επιστημονικό άρθρο (el)
- научна статия (bg)
- научная статья (ru)
- научни чланак (sr)
- מאמר מדעי (he)
- სამეცნიერო სტატია (ka)
- บทความทางวิทยาศาสตร์ (th)
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- bài báo khoa học (vi)
- naučni članak (sr-el)
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- научни чланак (sr-ec)
- article scientifique (fr)
- বৈজ্ঞানিক নিবন্ধ (bn)
- 2010 nî lūn-bûn (nan)
- 2010年の論文 (ja)
- 2010年論文 (zh-hk)
- 2010年論文 (zh-tw)
- 2010年論文 (zh-hant)
- 2010年論文 (yue)
- 2010年論文 (zh-mo)
- 2010年论文 (zh)
- 2010年论文 (zh-cn)
- 2010年论文 (zh-sg)
- 2010年论文 (zh-hans)
- 2010年论文 (wuu)
- 2010年论文 (zh-my)
- 2010년 논문 (ko)
- artículu científicu espublizáu en 2010 (ast)
- наукова стаття, опублікована в липні 2010 (uk)
- مقالة علمية نشرت في يوليو 2010 (ar)
- scientific article published on July 2010 (en)
- scientific article published on July 2010 (en-ca)
- scientific article published on July 2010 (en-gb)
|
| publication date
| |
| publication date
| |
| cites work
| |
| cites work
| - Short stature, mental retardation, and hypoparathyroidism: a new syndrome
- A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features
- Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43
- Syndrome of hypoparathyroidism, growth hormone deficiency, and multiple minor anomalies.
- Congenital hypoparathyroidism, seizure, extreme growth failure with developmental delay and dysmorphic features--another case of this new syndrome
- Confirmation of the assignment of the Sanjad-Sakati (congenital hypoparathyroidism) syndrome (OMIM 241410) locus to chromosome lq42-43.
- Sanjad-Sakati syndrome/Kenny-Caffey syndrome type 1: a study of 21 cases in Kuwait.
|
| author name string
| |
| author name string
| - Saif Al-Yaarubi
- Bushra Rafique
|
| rdfs:label
| - Sanjad-Sakati Syndrome in Omani children (en)
- Sanjad-Sakati Syndrome in Omani children (nl)
- Sanjad-Sakati Syndrome in Omani children (ast)
|
| skos:prefLabel
| - Sanjad-Sakati Syndrome in Omani children (en)
- Sanjad-Sakati Syndrome in Omani children (nl)
- Sanjad-Sakati Syndrome in Omani children (ast)
|
| name
| - Sanjad-Sakati Syndrome in Omani children (en)
- Sanjad-Sakati Syndrome in Omani children (nl)
- Sanjad-Sakati Syndrome in Omani children (ast)
|
| title
| |
| title
| - Sanjad-Sakati Syndrome in Omani children (en)
|
| page(s)
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| page(s)
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| instance of
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| instance of
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| main subject
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| main subject
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| PubMed ID
| |
| PubMed ID
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