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Journal Abstract Search

250 related items for PubMed ID: 16832598

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  • 3. Diagnosis of the Meckel-Gruber syndrome at eleven to fourteen weeks' gestation.
    Sepulveda W, Sebire NJ, Souka A, Snijders RJ, Nicolaides KH.
    Am J Obstet Gynecol; 1997 Feb; 176(2):316-9. PubMed ID: 9065174
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  • 4. First-trimester ultrasound diagnosis of Meckel-Grüber syndrome.
    Liu SS, Cheong ML, She BQ, Tsai MS.
    Acta Obstet Gynecol Scand; 2006 Feb; 85(6):757-9. PubMed ID: 16752273
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  • 5. Meckel-Gruber syndrome: ultrasonographic and fetal autopsy correlation.
    Khurana S, Saini V, Wadhwa V, Kaur H.
    J Ultrasound; 2017 Jun; 20(2):167-170. PubMed ID: 28593008
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  • 6. Antenatal ultrasonic diagnosis of Meckel Gruber syndrome (a case report with review of literature).
    Vernekar JA, Mishra GK, Pinto RG, Bhandari M, Mishra M.
    Australas Radiol; 1991 May; 35(2):186-8. PubMed ID: 1930022
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  • 7. Meckel-Gruber syndrome associated with short limbed dwarfism.
    Malguria N, Merchant SA, Kiran KV, Verghese SL.
    J Postgrad Med; 1996 May; 42(2):55-6. PubMed ID: 9715303
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  • 8. Meckel Gruber syndrome: a first trimester diagnosis of a recurrent case.
    Tanriverdi HA, Hendrik HJ, Ertan K, Schmidt W.
    Eur J Ultrasound; 2002 Jun; 15(1-2):69-72. PubMed ID: 12044856
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  • 9. Meckel Gruber syndrome, A case report.
    Aslan K, Külahçı Aslan E, Orhan A, Atalay MA.
    Organogenesis; 2015 Jun; 11(2):87-92. PubMed ID: 26037304
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  • 15. Meckel-Grüber syndrome: sonography and pathology.
    Ickowicz V, Eurin D, Maugey-Laulom B, Didier F, Garel C, Gubler MC, Laquerrière A, Avni EF.
    Ultrasound Obstet Gynecol; 2006 Mar; 27(3):296-300. PubMed ID: 16450359
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  • 18. [Meckel Gruber syndrome: about a rare case].
    Itchimouh S, Khabtou K, Mahdaoui S, Boufettal H, Samouh N.
    Pan Afr Med J; 2016 Mar; 25():43. PubMed ID: 28154732
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  • 19. Prenatal diagnosis of Meckel syndrome: a case report.
    Tongsong T, Piyamongkol W, Pongsatha S.
    J Obstet Gynaecol Res; 1999 Oct; 25(5):339-42. PubMed ID: 10533329
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  • 20. Meckel syndrome: prenatal ultrasonographic diagnosis in two cases showing marked differences in phenotypic expression.
    Gallimore AP, Davies PF.
    Australas Radiol; 1992 Feb; 36(1):62-4. PubMed ID: 1632751
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