(Q48490211)

12 February 2018

title

Trisomy 12p and epilepsy with myoclonic absences (English)

1 reference

12 February 2018

epilepsy with myoclonic absences

main subject

0 references

1 reference

1

1 reference

12 February 2018

Sebastiano Antonino Musumeci

series ordinal

2

1 reference

12 February 2018

Raffaele Ferri

series ordinal

3

1 reference

12 February 2018

author name string

Cammarata M

series ordinal

4

1 reference

12 February 2018

publication date

1 March 1998

1 reference

12 February 2018

published in

Brain and Development

1 reference

12 February 2018

volume

20

1 reference

12 February 2018

issue

2

1 reference

12 February 2018

page(s)

127-130

1 reference

12 February 2018

Identification of partial 12 trisomy by quinacrine fluorescence

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

Cytogenetic and molecular analysis in trisomy 12p.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

Partial trisomy 12p due to t(12;21)pat translocation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

Gene dosage effect for human triosephosphate isomerase and glyceraldehyde-3-phosphate dehydrogenase in partial trisomy 12p13 and trisomy 18p

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

Trisomy 12p syndrome: de novo occurrence of mosaic trisomy 12p in a mentally retarded boy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

Two cases of trisomy 12p due to rcpt(12;21)(p11;p11) inherited through three generations

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

New chromosomal dysmorphic syndromes. 4. Trisomy 12p.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

Trisomy 12p syndrome: a chromosomal disorder associated with generalized 3-Hz spike and wave discharges

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

Distal 8p deletion (8p23.1----8pter): a common deletion?

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

A newborn child with karyotype 47,XX,+der(12 (12pter leads to 12q12::9q24 leads to 8qter),t(8;12) (q24;q12) pat

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900006-0

7 January 2021

10.1016/S0387-7604(98)00006-0

Identifiers

DOI

1 reference

12 February 2018

1 reference

12 February 2018