Otten BJ - Search Results

1

Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings.

Hamel BC, Smits AP, Otten BJ, van den Helm B, Ropers HH, Mariman EC. Hamel BC, et al. Among authors: otten bj. Am J Med Genet. 1996 Jul 12;64(1):35-41. doi: 10.1002/(SICI)1096-8628(19960712)64:1<35::AID-AJMG5>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8826446 Free article.

2

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: otten bj. Hum Mol Genet. 1993 Nov;2(11):1779-83. doi: 10.1093/hmg/2.11.1779. Hum Mol Genet. 1993. PMID: 8281137

3

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation.

Kotzot D, Schmitt S, Bernasconi F, Robinson WP, Lurie IW, Ilyina H, Méhes K, Hamel BC, Otten BJ, Hergersberg M, et al. Kotzot D, et al. Among authors: otten bj. Hum Mol Genet. 1995 Apr;4(4):583-7. doi: 10.1093/hmg/4.4.583. Hum Mol Genet. 1995. PMID: 7633407 Free article.

4

A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty.

Kremer H, Martens JW, van Reen M, Verhoef-Post M, Wit JM, Otten BJ, Drop SL, Delemarre-van de Waal HA, Pombo-Arias M, De Luca F, Potau N, Buckler JM, Jansen M, Parks JS, Latif HA, Moll GW, Epping W, Saggese G, Mariman EC, Themmen AP, Brunner HG. Kremer H, et al. Among authors: otten bj. J Clin Endocrinol Metab. 1999 Mar;84(3):1136-40. doi: 10.1210/jcem.84.3.5515. J Clin Endocrinol Metab. 1999. PMID: 10084607

5

[Congenital hydrocephalus, oligophrenia, dwarfism, centripetal obesity and hypogonadism; an X-linked recessive hereditary illness?].

Sengers RC, Hamel BC, Otten BJ, van Gils JF, de Pagter AG. Sengers RC, et al. Among authors: otten bj. Tijdschr Kindergeneeskd. 1985 Feb;53(1):31-4. Tijdschr Kindergeneeskd. 1985. PMID: 4039476 Dutch.

6

Immunological tolerance in an HLA non-identical chimeric twin.

Viëtor HE, Hamel BC, van Bree SP, van der Meer EM, Smeets DF, Otten BJ, Holl RA, Claas FH. Viëtor HE, et al. Among authors: otten bj. Hum Immunol. 2000 Mar;61(3):190-2. doi: 10.1016/s0198-8859(99)00183-4. Hum Immunol. 2000. PMID: 10689108

7

Parents' perspectives on the unforeseen finding of a fetal sex chromosomal aneuploidy.

Pieters JJ, Kooper AJ, Eggink AJ, Verhaak CM, Otten BJ, Braat DD, Smits AP, van Leeuwen E. Pieters JJ, et al. Among authors: otten bj. Prenat Diagn. 2011 Mar;31(3):286-92. doi: 10.1002/pd.2707. Epub 2011 Feb 4. Prenat Diagn. 2011. PMID: 21294136

8

Maternal uniparental disomy 7--review and further delineation of the phenotype.

Kotzot D, Balmer D, Baumer A, Chrzanowska K, Hamel BC, Ilyina H, Krajewska-Walasek M, Lurie IW, Otten BJ, Schoenle E, Tariverdian G, Schinzel A. Kotzot D, et al. Among authors: otten bj. Eur J Pediatr. 2000 Apr;159(4):247-56. doi: 10.1007/s004310050064. Eur J Pediatr. 2000. PMID: 10789928

9

Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type II.

Kempers MJ, van der Crabben SN, de Vroede M, Alfen-van der Velden J, Netea-Maier RT, Duim RA, Otten BJ, Losekoot M, Wit JM. Kempers MJ, et al. Among authors: otten bj. Horm Res Paediatr. 2013;80(6):390-6. doi: 10.1159/000355403. Epub 2013 Nov 23. Horm Res Paediatr. 2013. PMID: 24280736

10

Antibody deficiency and isolated growth hormone deficiency in a girl with Mulibrey nanism.

Haraldsson A, van der Burgt CJ, Weemaes CM, Otten B, Bakkeren JA, Stoelinga GB. Haraldsson A, et al. Eur J Pediatr. 1993 Jun;152(6):509-12. doi: 10.1007/BF01955061. Eur J Pediatr. 1993. PMID: 8335020

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