A novel mutation causing pseudohypoparathyroidism 1A with congenital hypothyroidism and osteoma cutis.
about
Postnatal establishment of allelic Gαs silencing as a plausible explanation for delayed onset of parathyroid hormone resistance owing to heterozygous Gαs disruptionIdentification of a novel mutation in a patient with pseudohypoparathyroidism type Ia.Cognitive and behavioral phenotype of children with pseudohypoparathyroidism type 1A.
P2860
A novel mutation causing pseudohypoparathyroidism 1A with congenital hypothyroidism and osteoma cutis.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
A novel mutation causing pseud ...... othyroidism and osteoma cutis.
@en
type
label
A novel mutation causing pseud ...... othyroidism and osteoma cutis.
@en
prefLabel
A novel mutation causing pseud ...... othyroidism and osteoma cutis.
@en
P2093
P2860
P356
P1476
A novel mutation causing pseud ...... pothyroidism and osteoma cutis
@en
P2093
Maria Garzon
Tamar Lubell
P2860
P304
P356
10.4274/JCRPE.V1I5.244
P577
2009-08-06T00:00:00Z