Developmental profile in a patient with monosomy 10q and dup(17p) associated with a peripheral neuropathy.
about
Charcot-Marie-Tooth polyneuropathy: duplication, gene dosage, and genetic heterogeneity.Molecular mechanisms for CMT1A duplication and HNPP deletion.Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosome.DNA rearrangements on both homologues of chromosome 17 in a mildly delayed individual with a family history of autosomal dominant carpal tunnel syndrome
P2860
Developmental profile in a patient with monosomy 10q and dup(17p) associated with a peripheral neuropathy.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh-hant
name
Developmental profile in a patient with monosomy 10q and dup
@nl
Developmental profile in a pat ...... with a peripheral neuropathy.
@en
type
label
Developmental profile in a patient with monosomy 10q and dup
@nl
Developmental profile in a pat ...... with a peripheral neuropathy.
@en
prefLabel
Developmental profile in a patient with monosomy 10q and dup
@nl
Developmental profile in a pat ...... with a peripheral neuropathy.
@en
P2093
P2860
P1476
Developmental profile in a pat ...... with a peripheral neuropathy.
@en
P2093
Pellegrino JE
Pellegrino L
Spinner NB
P2860
P304
P356
10.1002/(SICI)1096-8628(19960202)61:4<377::AID-AJMG13>3.0.CO;2-P
P577
1996-02-01T00:00:00Z