Mariman E - Search Results

1

Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifida.

Morrison K, Papapetrou C, Attwood J, Hol F, Lynch SA, Sampath A, Hamel B, Burn J, Sowden J, Stott D, Mariman E, Edwards YH. Morrison K, et al. Among authors: mariman e. Hum Mol Genet. 1996 May;5(5):669-74. doi: 10.1093/hmg/5.5.669. Hum Mol Genet. 1996. PMID: 8733136

2

Mapping a gene for Noonan syndrome to the long arm of chromosome 12.

Jamieson CR, van der Burgt I, Brady AF, van Reen M, Elsawi MM, Hol F, Jeffery S, Patton MA, Mariman E. Jamieson CR, et al. Among authors: mariman e. Nat Genet. 1994 Dec;8(4):357-60. doi: 10.1038/ng1294-357. Nat Genet. 1994. PMID: 7894486

3

A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36.

Lynch SA, Bond PM, Copp AJ, Kirwan WO, Nour S, Balling R, Mariman E, Burn J, Strachan T. Lynch SA, et al. Among authors: mariman e. Nat Genet. 1995 Sep;11(1):93-5. doi: 10.1038/ng0995-93. Nat Genet. 1995. PMID: 7550324 Free article.

4

Clinical and molecular studies in a large Dutch family with Noonan syndrome.

van der Burgt I, Berends E, Lommen E, van Beersum S, Hamel B, Mariman E. van der Burgt I, et al. Among authors: mariman e. Am J Med Genet. 1994 Nov 1;53(2):187-91. doi: 10.1002/ajmg.1320530213. Am J Med Genet. 1994. PMID: 7856646

5

Methionine synthase and neural tube defects.

Morrison K, Edwards YH, Lynch SA, Burn J, Hol F, Mariman E. Morrison K, et al. Among authors: mariman e. J Med Genet. 1997 Nov;34(11):958. doi: 10.1136/jmg.34.11.958. J Med Genet. 1997. PMID: 9391898 Free PMC article. No abstract available.

6

Cosegregation of missense mutations of the luteinizing hormone receptor gene with familial male-limited precocious puberty.

Kremer H, Mariman E, Otten BJ, Moll GW Jr, Stoelinga GB, Wit JM, Jansen M, Drop SL, Faas B, Ropers HH, et al. Kremer H, et al. Among authors: mariman e. Hum Mol Genet. 1993 Nov;2(11):1779-83. doi: 10.1093/hmg/2.11.1779. Hum Mol Genet. 1993. PMID: 8281137

7

Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12.

Brady AF, Jamieson CR, van der Burgt I, Crosby A, van Reen M, Kremer H, Mariman E, Patton MA, Jeffery S. Brady AF, et al. Among authors: mariman e. Eur J Hum Genet. 1997 Sep-Oct;5(5):336-7. Eur J Hum Genet. 1997. PMID: 9412792 No abstract available.

8

Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription.

Riesewijk AM, Schepens MT, Welch TR, van den Berg-Loonen EM, Mariman EM, Ropers HH, Kalscheuer VM. Riesewijk AM, et al. Among authors: mariman em. Genomics. 1996 Jan 15;31(2):158-66. doi: 10.1006/geno.1996.0027. Genomics. 1996. PMID: 8824797

9

No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissues.

Jansen G, Bartolomei M, Kalscheuer V, Merkx G, Wormskamp N, Mariman E, Smeets D, Ropers HH, Wieringa B. Jansen G, et al. Among authors: mariman e. Hum Mol Genet. 1993 Aug;2(8):1221-7. doi: 10.1093/hmg/2.8.1221. Hum Mol Genet. 1993. PMID: 8401505

10

The MAS proto-oncogene is not imprinted in humans.

Riesewijk AM, Schepens MT, Mariman EM, Ropers HH, Kalscheuer VM. Riesewijk AM, et al. Among authors: mariman em. Genomics. 1996 Jul 15;35(2):380-2. doi: 10.1006/geno.1996.0372. Genomics. 1996. PMID: 8661154 Free article.

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