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1
Massive congenital depression of neonate’s skull
Massive congenital depression of neonate’s skull
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Massive congenital depression of neonate’s skull

Letouzey, Mathilde ; Berveiller, Paul

Archives of disease in childhood. Fetal and neonatal edition, 2018-07, Vol.103 (4), p.F316-F316 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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2
Helmet therapy in infants with positional skull deformation: randomised controlled trial
Helmet therapy in infants with positional skull deformation: randomised controlled trial
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Helmet therapy in infants with positional skull deformation: randomised controlled trial

van Wijk, Renske M ; van Vlimmeren, Leo A ; Groothuis-Oudshoorn, Catharina G M ; Van der Ploeg, Catharina P B ; IJzerman, Maarten J ; Boere-Boonekamp, Magda M

BMJ (Online), 2014-05, Vol.348 (may01 8), p.g2741-g2741 [Periódico revisado por pares]

England: British Medical Journal Publishing Group

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3
Imaging in craniosynostosis
Imaging in craniosynostosis
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Imaging in craniosynostosis

Rodgers, Anna ; Hopper, Neil

Archives of disease in childhood, 2014-01, Vol.99 (1), p.73-73 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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4
Holoprosencephaly with premaxillary agenesis in a prehistoric skull
Holoprosencephaly with premaxillary agenesis in a prehistoric skull
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Holoprosencephaly with premaxillary agenesis in a prehistoric skull

Pachajoa, Harry ; Rodriguez, Carlos A

Archives of disease in childhood. Fetal and neonatal edition, 2013-05, Vol.98 (3), p.264-264 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

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5
WTX mutations can occur both early and late in the pathogenesis of Wilms tumour
WTX mutations can occur both early and late in the pathogenesis of Wilms tumour
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WTX mutations can occur both early and late in the pathogenesis of Wilms tumour

Fukuzawa, Ryuji ; Holman, Sarah K ; Chow, C W ; Savarirayan, Ravi ; Reeve, Anthony E ; Robertson, Stephen P

Journal of medical genetics, 2010-11, Vol.47 (11), p.791-794 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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6
Congenital depression of the skull in a neonate
Congenital depression of the skull in a neonate
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Congenital depression of the skull in a neonate

Tayeh, Christelle ; Bali, Bassel ; Milad, Nadine ; Najjar, Marwan

BMJ case reports, 2016-09, Vol.2016, p.bcr2016215437 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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7
Hair-on-end appearance in a case of thalassemia intermedia
Hair-on-end appearance in a case of thalassemia intermedia
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Hair-on-end appearance in a case of thalassemia intermedia

Balikar, Riya ; Redkar, Neelam Narendra ; Patil, Meenakshi Amit ; Pillai, Rajit

BMJ case reports, 2013-01, Vol.2013, p.bcr2012008095 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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8
Down syndrome—novel associations: antenatal strawberry-shaped skull, severe neonatal hepatitis and an unusual form of portosystemic hepatic shunt
Down syndrome—novel associations: antenatal strawberry-shaped skull, severe neonatal hepatitis and an unusual form of portosystemic hepatic shunt
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Down syndrome—novel associations: antenatal strawberry-shaped skull, severe neonatal hepatitis and an unusual form of portosystemic hepatic shunt

Losa, Ignatius ; Owoeye, Adedayo

BMJ case reports, 2015-10, Vol.2015, p.bcr2015212852 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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9
A case of craniofacial fibrous dysplasia associated with McCune-Albright syndrome lost to follow-up
A case of craniofacial fibrous dysplasia associated with McCune-Albright syndrome lost to follow-up
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A case of craniofacial fibrous dysplasia associated with McCune-Albright syndrome lost to follow-up

Williams, Robert Gareth Michael

BMJ case reports, 2015-02, Vol.2015, p.bcr2014209011 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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10
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)
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The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)

Wuyts, Wim ; Cleiren, Erna ; Homfray, Tessa ; Rasore-Quartino, Alberto ; Vanhoenacker, Filip ; Van Hul, Wim

Journal of medical genetics, 2000-12, Vol.37 (12), p.916-920 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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