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166 related items for PubMed ID: 464411
1. [Meckel syndrome (author's transl)]. Alonso JA, Gómez Castillo E, Arribas M, Luque R, Rubio C. An Esp Pediatr; 1979 May; 12(5):403-10. PubMed ID: 464411 [Abstract] [Full Text] [Related]
2. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome. Hsia YE, Appadorai V, Breg WR, Howard RO. Birth Defects Orig Artic Ser; 1974 May; 10(8):19-25. PubMed ID: 4142400 [No Abstract] [Full Text] [Related]
3. Meckel-Gruber syndrome. A lethal combination of abnormalities. Coard KC, Escoffery CT. West Indian Med J; 1990 Mar; 39(1):52-6. PubMed ID: 2333699 [Abstract] [Full Text] [Related]
5. [2 new cases of Meckel-Gruber syndrome in the same family]. Franzoni R, Scalercio A. Minerva Pediatr; 1986 Sep 30; 38(17-18):783-9. PubMed ID: 3796537 [No Abstract] [Full Text] [Related]
6. [Three new cases of Meckel's syndrome or Gruber's splanchnocystic dysencephaly in siblings. Anatomo-pathologic and cytogenetic study. Nosologic discussion]. Naffah J, Ghosn G, Gharios N. Arch Fr Pediatr; 1972 Dec 30; 29(10):1069-81. PubMed ID: 4662280 [No Abstract] [Full Text] [Related]
7. The Meckel syndrome: clinicopathological findings in 67 patients. Salonen R. Am J Med Genet; 1984 Aug 30; 18(4):671-89. PubMed ID: 6486167 [Abstract] [Full Text] [Related]
8. [Meckel syndrome in 2 brothers. Clinical, anatomopathologic and genetic aspects]. Restrepo CM, García-Cruz D, Sánchez G, Cantú JM. Bol Med Hosp Infant Mex; 1988 Sep 30; 45(9):600-4. PubMed ID: 3190852 [No Abstract] [Full Text] [Related]
9. Polydactyly in a carrier of the gene for the Meckel syndrome. Nelson J, Nevin NC, Hanna EJ. Am J Med Genet; 1994 Nov 15; 53(3):207-9. PubMed ID: 7856653 [Abstract] [Full Text] [Related]
10. [The Meckel-syndrome in a newborn]. Göcke H, Muradow I, Eldering G, Gullotta F. Geburtshilfe Frauenheilkd; 1982 Aug 15; 42(8):602-4. PubMed ID: 6922811 [No Abstract] [Full Text] [Related]
11. [Contribution to information and genetic counseling in Mekkel's syndrome (author's transl)]. Koch G, Schwanitz G. MMW Munch Med Wochenschr; 1975 Oct 24; 117(43):1723-4. PubMed ID: 52836 [Abstract] [Full Text] [Related]
12. Gross anatomical studies of a newborn infant with the Meckel syndrome. Pettersen JC. Am J Med Genet; 1984 Aug 24; 18(4):649-59. PubMed ID: 6486165 [Abstract] [Full Text] [Related]
13. Meckel-Gruber syndrome. Ramachandran U, Malla T, Joshi KS. Kathmandu Univ Med J (KUMJ); 2006 Aug 24; 4(3):334-6. PubMed ID: 18603929 [Abstract] [Full Text] [Related]
14. Prenatal diagnosis of Meckel-Gruber syndrome and Dandy-Walker malformation in four consecutive affected siblings, with the fourth one being diagnosed prenatally at 22 weeks of gestation. Balci S, Tekşen F, Dökmeci F, Cengiz B, Cömert RB, Can B, Ozdamar S. Turk J Pediatr; 2004 Aug 24; 46(3):283-8. PubMed ID: 15503488 [Abstract] [Full Text] [Related]
15. Dandy-Walker malformation in the Meckel syndrome. Herriot R, Hallam LA, Gray ES. Am J Med Genet; 1991 May 01; 39(2):207-10. PubMed ID: 2063927 [Abstract] [Full Text] [Related]
16. Dandy-Walker malformation (variant), cystic dysplastic kidneys, and hepatic fibrosis: a distinct entity or Meckel syndrome? Walpole IR, Goldblatt J, Hockey A, Knowles S. Am J Med Genet; 1991 Jun 01; 39(3):294-8. PubMed ID: 1867280 [Abstract] [Full Text] [Related]
18. Genetics of the Meckel syndrome (dysencephalia splanchnocystica). Hsia YE, Bratu M, Herbordt A. Pediatrics; 1971 Aug 01; 48(2):237-47. PubMed ID: 4997860 [No Abstract] [Full Text] [Related]
19. [Ultrasonic diagnosis of a hereditary multiple malformation syndrome: Meckel-Gruber syndrome or Carpenter-Hunter syndrome]. Adjahoto EO, De Grandi P, Maillard-Brignon C, Pescia G. J Gynecol Obstet Biol Reprod (Paris); 1992 Aug 01; 21(8):928-33. PubMed ID: 1491139 [Abstract] [Full Text] [Related]
20. Meckel syndrome in different populations. Lurie IW, Prytkov AN, Meldere LV. Am J Med Genet; 1984 Aug 01; 18(4):661-9. PubMed ID: 6486166 [Abstract] [Full Text] [Related] Page: [Next] [New Search]