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Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2).
Eur J Paediatr Neurol. 2003;7(1):5-12. doi: 10.1016/s1090-3798(02)00134-4.
Eur J Paediatr Neurol. 2003.
PMID: 12615169
Review.
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. Among authors: schoonbrood lenssen am.
Genet Couns. 1998;9(3):211-3.
Genet Couns. 1998.
PMID: 9777344
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Wolf-Hirschhorn (4P-) syndrome in adults.
Marcelis C, Schrander-Stumpel C, Engelen J, Schoonbrood-Lenssen A, Willemse A, Beemer F, Sigaudy S, Missirian C, Philip N, Fryns JP.
Marcelis C, et al.
Genet Couns. 2001;12(1):35-48.
Genet Couns. 2001.
PMID: 11332977
Review.
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Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
Hamel BC, Mariman EC, van Beersum SE, Schoonbrood-Lenssen AM, Ropers HH.
Hamel BC, et al. Among authors: schoonbrood lenssen am.
Am J Med Genet. 1994 Jul 15;51(4):591-7. doi: 10.1002/ajmg.1320510459.
Am J Med Genet. 1994.
PMID: 7943045
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