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Literature DB >> 1613765

Meckel syndrome and neural tube defects in Kuwait.

A S Teebi, Q A al Saleh, H Odeh.

Abstract

Entities: Disease

Mesh：

Year: 1992 PMID： 1613765 PMCID： PMC1015870 DOI： 10.1136/jmg.29.2.140-a

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

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9 in total

1. Phenotypic variability in Meckel-Gruber syndrome.

Authors: T I Farag; R Usha; R Uma; S A Mady; K al-Nagdy; M H el-Badramany
Journal: Clin Genet Date: 1990-09 Impact factor: 4.438

2. Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population.

Authors: T I Farag; A S Teebi
Journal: Clin Genet Date: 1988-02 Impact factor: 4.438

3. Anencephaly: a vanishing problem in Bedouins?

Authors: T I Farag; S A al-Awadi; S Yassin; T A el-Kassaby; S Jaefary; R Usha; R Uma; S A Mady; M Fakhr; M Mannae
Journal: J Med Genet Date: 1989-08 Impact factor: 6.318

4. Anencephaly: disappearing in Kuwait?

Authors: S A Al-Awadi; T I Farag; A S Teebi; K K Naguib; M Y El-Khalifa
Journal: Lancet Date: 1984-09-22 Impact factor: 79.321

5. High incidence of Meckel's syndrome in Gujarati Indians.

Authors: I D Young; A B Rickett; M Clarke
Journal: J Med Genet Date: 1985-08 Impact factor: 6.318

6. Phenotypic variation in Meckel syndrome.

Authors: M J Seller
Journal: Clin Genet Date: 1981-07 Impact factor: 4.438

7. Meckel syndrome in different populations.

Authors: I W Lurie; A N Prytkov; L V Meldere
Journal: Am J Med Genet Date: 1984-08

8. The Meckel syndrome: clinicopathological findings in 67 patients.

Authors: R Salonen
Journal: Am J Med Genet Date: 1984-08

9. Nonsyndromal anencephaly: possible autosomal recessive variant.

Authors: T I Farag; A S Teebi; S A Al-Awadi
Journal: Am J Med Genet Date: 1986-07

9 in total

Review 1. The Finnish Disease Heritage III: the individual diseases.

Authors: Reijo Norio
Journal: Hum Genet Date: 2003-03-08 Impact factor: 4.132

2. Meckel-Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe.

Authors: Ingeborg Barisic; Ljubica Boban; Maria Loane; Ester Garne; Diana Wellesley; Elisa Calzolari; Helen Dolk; Marie-Claude Addor; Jorieke Eh Bergman; Paula Braz; Elizabeth S Draper; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Anna Pierini; Annette Queisser-Luft; Judith Rankin; Anke Rissmann; Christine Verellen-Dumoulin
Journal: Eur J Hum Genet Date: 2014-09-03 Impact factor: 4.246

3. Comparative physical maps of the human and mouse Meckel syndrome critical regions.

Authors: Kathryn E Hentges; Mira Kyttälä; Monica J Justice; Leena Peltonen
Journal: Mamm Genome Date: 2004-04 Impact factor: 2.957

Review 4. Meckel syndrome.

Authors: R Salonen; P Paavola
Journal: J Med Genet Date: 1998-06 Impact factor: 6.318