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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 1 |
2003 | 1 |
2009 | 2 |
2013 | 1 |
2024 | 0 |
PubMed (cited) for id: 615465
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Page 1
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
J Med Genet. 2013 Sep;50(9):585-92. doi: 10.1136/jmedgenet-2013-101603. Epub 2013 Jun 28.
J Med Genet. 2013.
PMID: 23812909
Free PMC article.
Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: further delineation and review.
Vilain C, Mortier G, Van Vliet G, Dubourg C, Heinrichs C, de Silva D, Verloes A, Baumann C.
Vilain C, et al.
Am J Med Genet A. 2009 Jul;149A(7):1476-81. doi: 10.1002/ajmg.a.32678.
Am J Med Genet A. 2009.
PMID: 19504604
Free article.
Review.
Item in Clipboard
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes.
Zechi-Ceide RM, Ribeiro LA, Raskin S, Bertolacini CD, Guion-Almeida ML, Richieri-Costa A.
Zechi-Ceide RM, et al.
Am J Med Genet A. 2009 Jun;149A(6):1277-9. doi: 10.1002/ajmg.a.32844.
Am J Med Genet A. 2009.
PMID: 19449411
Item in Clipboard
Holoprosencephaly, bilateral cleft lip and palate and ectrodactyly: another case and follow up.
König R, Beeg T, Tariverdian G, Scheffer H, Bitter K.
König R, et al.
Clin Dysmorphol. 2003 Oct;12(4):221-5. doi: 10.1097/00019605-200310000-00002.
Clin Dysmorphol. 2003.
PMID: 14564207
Item in Clipboard
Holoprosencephaly, telecanthus and ectrodactyly: a second case.
Young ID, Zuccollo JM, Barrow M, Fowlie A.
Young ID, et al.
Clin Dysmorphol. 1992 Jan;1(1):47-51.
Clin Dysmorphol. 1992.
PMID: 1342859
Review.
No abstract available.
Item in Clipboard
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