Meacham syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Meacham syndrome" in English language version.

refsWebsite

Global rank English rank

5nih.gov

4^th place

4doi.org

2^nd place

4worldcat.org

5^th place

3omim.org

4,380^th place

4,305^th place

2semanticscholar.org

11^th place

8^th place

1web.archive.org

1^st place

1orpha.net

3,537^th place

7,177^th place

1mendelian.co

low place

doi.org

Suri, Mohnish; Kelehan, Peter; O'neill, David; Vadeyar, Shantala; Grant, Judith; Ahmed, S. Faisal; Tolmie, John; McCann, Emma; Lam, Wayne; Smith, Shirley; Fitzpatrick, David (2007-10-01). "WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations". American Journal of Medical Genetics. Part A. 143A (19): 2312–2320. doi:10.1002/ajmg.a.31924. ISSN 1552-4825. PMID 17853480. S2CID 20548643.
Meacham, L. R.; Winn, K. J.; Culler, F. L.; Parks, J. S. (1991-12-15). "Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype". American Journal of Medical Genetics. 41 (4): 478–481. doi:10.1002/ajmg.1320410420. ISSN 0148-7299. PMID 1844355.
Killeen, Orla G.; Kelehan, Peter; Reardon, William (2002-01-01). "Double vagina with sex reversal, congenital diaphragmatic hernia, pulmonary and cardiac malformations--another case of Meacham syndrome". Clinical Dysmorphology. 11 (1): 25–28. doi:10.1097/00019605-200201000-00005. ISSN 0962-8827. PMID 11822701.
Suri, Mohnish; Kelehan, Peter; O'neill, David; Vadeyar, Shantala; Grant, Judith; Ahmed, S. Faisal; Tolmie, John; McCann, Emma; Lam, Wayne; Smith, Shirley; Fitzpatrick, David (2007-10-01). "WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations". American Journal of Medical Genetics. Part A. 143A (19): 2312–2320. doi:10.1002/ajmg.a.31924. ISSN 1552-4825. PMID 17853480. S2CID 20548643.

mendelian.co

"Meacham Syndrome". www.mendelian.co. 2022-06-29. Retrieved 2022-06-29.

nih.gov

pubmed.ncbi.nlm.nih.gov

Suri, Mohnish; Kelehan, Peter; O'neill, David; Vadeyar, Shantala; Grant, Judith; Ahmed, S. Faisal; Tolmie, John; McCann, Emma; Lam, Wayne; Smith, Shirley; Fitzpatrick, David (2007-10-01). "WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations". American Journal of Medical Genetics. Part A. 143A (19): 2312–2320. doi:10.1002/ajmg.a.31924. ISSN 1552-4825. PMID 17853480. S2CID 20548643.
Meacham, L. R.; Winn, K. J.; Culler, F. L.; Parks, J. S. (1991-12-15). "Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype". American Journal of Medical Genetics. 41 (4): 478–481. doi:10.1002/ajmg.1320410420. ISSN 0148-7299. PMID 1844355.
Killeen, Orla G.; Kelehan, Peter; Reardon, William (2002-01-01). "Double vagina with sex reversal, congenital diaphragmatic hernia, pulmonary and cardiac malformations--another case of Meacham syndrome". Clinical Dysmorphology. 11 (1): 25–28. doi:10.1097/00019605-200201000-00005. ISSN 0962-8827. PMID 11822701.
Suri, Mohnish; Kelehan, Peter; O'neill, David; Vadeyar, Shantala; Grant, Judith; Ahmed, S. Faisal; Tolmie, John; McCann, Emma; Lam, Wayne; Smith, Shirley; Fitzpatrick, David (2007-10-01). "WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations". American Journal of Medical Genetics. Part A. 143A (19): 2312–2320. doi:10.1002/ajmg.a.31924. ISSN 1552-4825. PMID 17853480. S2CID 20548643.

rarediseases.info.nih.gov

"Meacham Winn Culler syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 2023-01-04. Retrieved 2022-06-29.

omim.org

"OMIM Clinical Synopsis - #608978 - Meacham Syndrome". omim.org. Retrieved 2022-06-29.
"OMIM Entry - # 608978 - Meacham Syndrome". www.omim.org. Retrieved 2022-06-29.
"OMIM Entry - # 608978 - Meacham Syndrome". www.omim.org. Retrieved 2022-06-29.

orpha.net

"Orphanet: Meacham syndrome". www.orpha.net. Retrieved 2022-06-29.

semanticscholar.org

api.semanticscholar.org

Suri, Mohnish; Kelehan, Peter; O'neill, David; Vadeyar, Shantala; Grant, Judith; Ahmed, S. Faisal; Tolmie, John; McCann, Emma; Lam, Wayne; Smith, Shirley; Fitzpatrick, David (2007-10-01). "WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations". American Journal of Medical Genetics. Part A. 143A (19): 2312–2320. doi:10.1002/ajmg.a.31924. ISSN 1552-4825. PMID 17853480. S2CID 20548643.
Suri, Mohnish; Kelehan, Peter; O'neill, David; Vadeyar, Shantala; Grant, Judith; Ahmed, S. Faisal; Tolmie, John; McCann, Emma; Lam, Wayne; Smith, Shirley; Fitzpatrick, David (2007-10-01). "WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations". American Journal of Medical Genetics. Part A. 143A (19): 2312–2320. doi:10.1002/ajmg.a.31924. ISSN 1552-4825. PMID 17853480. S2CID 20548643.

web.archive.org

"Meacham Winn Culler syndrome - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Archived from the original on 2023-01-04. Retrieved 2022-06-29.

worldcat.org

search.worldcat.org

Suri, Mohnish; Kelehan, Peter; O'neill, David; Vadeyar, Shantala; Grant, Judith; Ahmed, S. Faisal; Tolmie, John; McCann, Emma; Lam, Wayne; Smith, Shirley; Fitzpatrick, David (2007-10-01). "WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations". American Journal of Medical Genetics. Part A. 143A (19): 2312–2320. doi:10.1002/ajmg.a.31924. ISSN 1552-4825. PMID 17853480. S2CID 20548643.
Meacham, L. R.; Winn, K. J.; Culler, F. L.; Parks, J. S. (1991-12-15). "Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype". American Journal of Medical Genetics. 41 (4): 478–481. doi:10.1002/ajmg.1320410420. ISSN 0148-7299. PMID 1844355.
Killeen, Orla G.; Kelehan, Peter; Reardon, William (2002-01-01). "Double vagina with sex reversal, congenital diaphragmatic hernia, pulmonary and cardiac malformations--another case of Meacham syndrome". Clinical Dysmorphology. 11 (1): 25–28. doi:10.1097/00019605-200201000-00005. ISSN 0962-8827. PMID 11822701.
Suri, Mohnish; Kelehan, Peter; O'neill, David; Vadeyar, Shantala; Grant, Judith; Ahmed, S. Faisal; Tolmie, John; McCann, Emma; Lam, Wayne; Smith, Shirley; Fitzpatrick, David (2007-10-01). "WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations". American Journal of Medical Genetics. Part A. 143A (19): 2312–2320. doi:10.1002/ajmg.a.31924. ISSN 1552-4825. PMID 17853480. S2CID 20548643.