A mouse model for hereditary thyroid dysgenesis and cleft palate (Q28513528)

10

0 references

author name string

M. De Felice

1

1 reference

25 January 2017

C. Ovitt

2

1 reference

25 January 2017

E. Biffali

3

1 reference

25 January 2017

A. Rodriguez-Mallon

4

1 reference

25 January 2017

K. Anastassiadis

6

1 reference

25 January 2017

P. E. Macchia

7

1 reference

25 January 2017

M. G. Mattei

8

1 reference

25 January 2017

A. Mariano

9

1 reference

25 January 2017

V. Macchia

11

1 reference

25 January 2017

R. Di Lauro

Comparison of Epidemiological Data on Congenital Hypothyroidism in Europe with Those of Other Parts in the World

12

1 reference

25 January 2017

language of work or name

English

0 references

publication date

1 August 1998

1 reference

25 January 2017

1 reference

25 January 2017

19

1 reference

25 January 2017

395–398

1 reference

25 January 2017

4

1 reference

25 January 2017

1 reference

7 January 2021

TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of differentiation

1 reference

7 January 2021

Hox group 3 paralogs regulate the development and migration of the thymus, thyroid, and parathyroid glands

1 reference

7 January 2021

Thyroid-specific gene expression

1 reference

7 January 2021

Thyroid Development and Disorders of Thyroid Function in the Newborn

1 reference

7 January 2021

The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary

1 reference

7 January 2021

Follicular cells of the thyroid gland require Pax8 gene function

1 reference

7 January 2021

Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction

1 reference

7 January 2021

Transforming growth factor-beta 3 is required for secondary palate fusion

1 reference

7 January 2021

Congenital hypothyroidism, spiky hair, and cleft palate

1 reference

7 January 2021

Syndromic association of cleft palate, bilateral choanal atresia, curly hair, and congenital hypothyroidism

1 reference

7 January 2021

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

1 reference

7 January 2021

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

1 reference

7 January 2021

Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland

1 reference

7 January 2021

Gene targeting in embryonic stem cells

1 reference

7 January 2021

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

1 reference

7 January 2021