Lalande M - Search Results

1

Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region.

Robinson WP, Lalande M. Robinson WP, et al. Among authors: lalande m. Hum Mol Genet. 1995 May;4(5):801-6. doi: 10.1093/hmg/4.5.801. Hum Mol Genet. 1995. PMID: 7633438 Free article.

2

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region.

Ozçelik T, Leff S, Robinson W, Donlon T, Lalande M, Sanjines E, Schinzel A, Francke U. Ozçelik T, et al. Among authors: lalande m. Nat Genet. 1992 Dec;2(4):265-9. doi: 10.1038/ng1292-265. Nat Genet. 1992. PMID: 1303277

3

Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene.

Buiting K, Dittrich B, Gross S, Greger V, Lalande M, Robinson W, Mutirangura A, Ledbetter D, Horsthemke B. Buiting K, et al. Among authors: lalande m. Hum Mol Genet. 1993 Dec;2(12):1991-4. doi: 10.1093/hmg/2.12.1991. Hum Mol Genet. 1993. PMID: 8111365

4

FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions.

Knoll JH, Sinnett D, Wagstaff J, Glatt K, Wilcox AS, Whiting PM, Wingrove P, Sikela JM, Lalande M. Knoll JH, et al. Among authors: lalande m. Hum Mol Genet. 1993 Feb;2(2):183-9. doi: 10.1093/hmg/2.2.183. Hum Mol Genet. 1993. PMID: 8388764

5

Linkage analysis in familial Angelman syndrome.

Wagstaff J, Shugart YY, Lalande M. Wagstaff J, et al. Among authors: lalande m. Am J Hum Genet. 1993 Jul;53(1):105-12. Am J Hum Genet. 1993. PMID: 8317476 Free PMC article.

6

Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons.

Langouët M, Glatt-Deeley HR, Chung MS, Dupont-Thibert CM, Mathieux E, Banda EC, Stoddard CE, Crandall L, Lalande M. Langouët M, et al. Among authors: lalande m. Hum Mol Genet. 2018 Feb 1;27(3):505-515. doi: 10.1093/hmg/ddx420. Hum Mol Genet. 2018. PMID: 29228278

7

Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3.

Greger V, Knoll JH, Wagstaff J, Woolf E, Lieske P, Glatt H, Benn PA, Rosengren SS, Lalande M. Greger V, et al. Among authors: lalande m. Am J Hum Genet. 1997 Mar;60(3):574-80. Am J Hum Genet. 1997. PMID: 9042916 Free PMC article.

8

Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.

Knoll JH, Nicholls RD, Magenis RE, Glatt K, Graham JM Jr, Kaplan L, Lalande M. Knoll JH, et al. Among authors: lalande m. Am J Hum Genet. 1990 Jul;47(1):149-54. Am J Hum Genet. 1990. PMID: 1971993 Free PMC article.

9

Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.

Knoll JH, Glatt KA, Nicholls RD, Malcolm S, Lalande M. Knoll JH, et al. Among authors: lalande m. Am J Hum Genet. 1991 Jan;48(1):16-21. Am J Hum Genet. 1991. PMID: 1985457 Free PMC article.

10

Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion.

Martins-Taylor K, Hsiao JS, Chen PF, Glatt-Deeley H, De Smith AJ, Blakemore AI, Lalande M, Chamberlain SJ. Martins-Taylor K, et al. Among authors: lalande m. Hum Mol Genet. 2014 May 1;23(9):2364-73. doi: 10.1093/hmg/ddt628. Epub 2013 Dec 20. Hum Mol Genet. 2014. PMID: 24363065 Free PMC article.

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