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Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.
Genet Med. 2021 Oct;23(10):2016. doi: 10.1038/s41436-021-01306-7.
Genet Med. 2021.
PMID: 34522029
Free article.
No abstract available.
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.
Rodan LH, Spillmann RC, Kurata HT, Lamothe SM, Maghera J, Jamra RA, Alkelai A, Antonarakis SE, Atallah I, Bar-Yosef O, Bilan F, Bjorgo K, Blanc X, Van Bogaert P, Bolkier Y, Burrage LC, Christ BU, Granadillo JL, Dickson P, Donald KA, Dubourg C, Eliyahu A, Emrick L, Engleman K, Gonfiantini MV, Good JM, Kalser J, Kloeckner C, Lachmeijer G, Macchiaiolo M, Nicita F, Odent S, O'Heir E, Ortiz-Gonzalez X, Pacio-Miguez M, Palomares-Bralo M, Pena L, Platzer K, Quinodoz M, Ranza E, Rosenfeld JA, Roulet-Perez E, Santani A, Santos-Simarro F, Pode-Shakked B, Skraban C, Slaugh R, Superti-Furga A, Thiffault I, van Jaabrsveld RH, Vincent M, Wang HG, Zacher P; Undiagnosed Diseases Network; Rush E, Pitt GS, Au PYB, Shashi V.
Rodan LH, et al. Among authors: lachmeijer g.
Genet Med. 2021 Oct;23(10):1922-1932. doi: 10.1038/s41436-021-01232-8. Epub 2021 Jun 23.
Genet Med. 2021.
PMID: 34163037
Free PMC article.
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Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging.
Deden C, Neveling K, Zafeiropopoulou D, Gilissen C, Pfundt R, Rinne T, de Leeuw N, Faas B, Gardeitchik T, Sallevelt SCEH, Paulussen A, Stevens SJC, Sikkel E, Elting MW, van Maarle MC, Diderich KEM, Corsten-Janssen N, Lichtenbelt KD, Lachmeijer G, Vissers LELM, Yntema HG, Nelen M, Feenstra I, van Zelst-Stams WAG.
Deden C, et al. Among authors: lachmeijer g.
Prenat Diagn. 2020 Jul;40(8):972-983. doi: 10.1002/pd.5717. Epub 2020 May 5.
Prenat Diagn. 2020.
PMID: 32333414
Free PMC article.
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Clinical and genetic characteristics for the Urofacial Syndrome (UFS).
Tu Y, Yang P, Yang J, Xu Y, Xiong F, Yu Q, Gu W, Pond D, Mendelsohn N, Lachmeijer GA, Zhang S, Wang CY.
Tu Y, et al. Among authors: lachmeijer ga.
Int J Clin Exp Pathol. 2014 Apr 15;7(5):1842-8. eCollection 2014.
Int J Clin Exp Pathol. 2014.
PMID: 24966895
Free PMC article.
Review.
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Failure to detect linkage of preeclampsia to the region of the NOS3 locus on chromosome 7q.
Lewis I, Lachmeijer G, Downing S, Dekker G, Glazebrook C, Clayton D, Morris NH, O'Shaughnessy KM.
Lewis I, et al. Among authors: lachmeijer g.
Am J Hum Genet. 1999 Jan;64(1):310-3. doi: 10.1086/302179.
Am J Hum Genet. 1999.
PMID: 9915975
Free PMC article.
No abstract available.
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