Monosomy1p36.3 and Trisomy 19p13.3 in a Child with Periventricular Nodular Heterotopia

Maria Descartes, et al; Maria Descartes

Monosomy1p36.3 and Trisomy 19p13.3 in a Child with Periventricular Nodular Heterotopia

Maria Descartes, et al, Maria Descartes

Research output: Contribution to journal › Article › peer-review

Original language	American English
Journal	Pediatric Neurology
Volume	45
State	Published - 2011

Disciplines

Medicine and Health Sciences

Cite this

@article{99b6697d44824eb7aa231797b7e759b9,

title = "Monosomy1p36.3 and Trisomy 19p13.3 in a Child with Periventricular Nodular Heterotopia",

author = "\{Descartes, et al\}, Maria and Maria Descartes",

note = "Monosomy 1p36 is a clinically recognizable syndrome that is considered to be the most common terminal deletion syndrome. It has characteristic clinical features that include craniofacial dysmorphism, congenital anomalies, hearing deficits, developmental delay, mental retardation, hypotonia, seizures, and brain anomalies. Brain anomalies in patients with 1p36 deletion are frequent but inconsistent.",

year = "2011",

language = "American English",

volume = "45",

journal = "Pediatric Neurology",

}

TY - JOUR

T1 - Monosomy1p36.3 and Trisomy 19p13.3 in a Child with Periventricular Nodular Heterotopia

AU - Descartes, et al, Maria

AU - Descartes, Maria

N1 - Monosomy 1p36 is a clinically recognizable syndrome that is considered to be the most common terminal deletion syndrome. It has characteristic clinical features that include craniofacial dysmorphism, congenital anomalies, hearing deficits, developmental delay, mental retardation, hypotonia, seizures, and brain anomalies. Brain anomalies in patients with 1p36 deletion are frequent but inconsistent.

PY - 2011

Y1 - 2011

UR - https://pubmed.ncbi.nlm.nih.gov/21907895/

M3 - Article

VL - 45

JO - Pediatric Neurology

JF - Pediatric Neurology

ER -

Monosomy1p36.3 and Trisomy 19p13.3 in a Child with Periventricular Nodular Heterotopia

Disciplines

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