Moog U - Search Results

1

The outcome of diagnostic studies on the etiology of mental retardation: considerations on the classification of the causes.

Moog U. Moog U. Am J Med Genet A. 2005 Aug 30;137(2):228-31. doi: 10.1002/ajmg.a.30841. Am J Med Genet A. 2005. PMID: 16086396 Review.

2

Oculocerebrocutaneous syndrome: report of three additional cases and aetiological considerations.

Moog U, de Die-Smulders C, Systermans JM, Cobben JM. Moog U, et al. Clin Genet. 1997 Oct;52(4):219-25. doi: 10.1111/j.1399-0004.1997.tb02551.x. Clin Genet. 1997. PMID: 9383027

3

Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?

Moog U, Bleeker-Wagemakers EM, Crobach P, Vles JS, Schrander-Stumpel CT. Moog U, et al. Am J Med Genet. 1998 Jul 7;78(3):263-6. Am J Med Genet. 1998. PMID: 9677063

4

Spasticity, mental retardation, macrocephaly and distinct craniofacial appearance: confirmation of a new subtype of complicated spastic paraplegia?

Moog U, Schoonbrood-Lenssen AM, Schrander-Stumpel CT, Fryns JP. Moog U, et al. Genet Couns. 1998;9(3):211-3. Genet Couns. 1998. PMID: 9777344

5

Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?

Moog U, Maroteaux P, Schrander-Stumpel CT, van Ooij A, Schrander JJ, Fryns JP. Moog U, et al. J Med Genet. 1999 Nov;36(11):856-8. J Med Genet. 1999. PMID: 10544232 Free PMC article.

6

Duplication of chromosome region 8p23.1-->p23.3: a benign variant?

Engelen JJ, Moog U, Evers JL, Dassen H, Albrechts JC, Hamers AJ. Engelen JJ, et al. Among authors: moog u. Am J Med Genet. 2000 Mar 6;91(1):18-21. Am J Med Genet. 2000. PMID: 10751083

7

Familial dup(8)(p12p21.1): mild phenotypic effect and review of partial 8p duplications.

Moog U, Engelen JJ, Albrechts JC, Baars LG, de Die-Smulders CE. Moog U, et al. Am J Med Genet. 2000 Oct 2;94(4):306-10. doi: 10.1002/1096-8628(20001002)94:4<306::aid-ajmg8>3.0.co;2-v. Am J Med Genet. 2000. PMID: 11038444 Review.

8

Acampomelic campomelic syndrome.

Moog U, Jansen NJ, Scherer G, Schrander-Stumpel CT. Moog U, et al. Am J Med Genet. 2001 Dec 1;104(3):239-45. Am J Med Genet. 2001. PMID: 11754051

9

Familial cryptic translocation with deletion 4q33-->4qter and duplication 7q34-->7qter in brothers with mental retardation, macrocephaly and iris coloboma.

Moog U, Engelen JJ, van Schrojenstein Lantman-de Valk HM, Driessen SD, Fryns JP. Moog U, et al. Clin Dysmorphol. 2003 Jan;12(1):35-9. doi: 10.1097/00019605-200301000-00006. Clin Dysmorphol. 2003. PMID: 12514363

10

Deletion of chromosome region 18q21.1 --> 18q21.3 in a patient without clinical features of the 18q- phenotype.

Engelen JJ, Moog U, Weber J, Haagen AA, van Uum CM, Hamers AJ. Engelen JJ, et al. Among authors: moog u. Am J Med Genet A. 2003 Jun 15;119A(3):356-9. doi: 10.1002/ajmg.a.10266. Am J Med Genet A. 2003. PMID: 12784305

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