(Q24319625)

embryonic digit morphogenesis

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Townes-Brocks syndrome

1 reference

J Kohlhase

1

0 references

A Wischermann

2

0 references

H Reichenbach

3

0 references

U Froster

4

0 references

W Engel

Hereditary syndrome of imperforate anus with hand, foot, and ear anomalies

5

0 references

language of work or name

English

0 references

publication date

January 1998

0 references

published in

Nature Genetics

0 references

volume

18

0 references

issue

1

0 references

page(s)

81-3

0 references

cites work

1 reference

Isolation, characterization, and organ-specific expression of two novel human zinc finger genes related to the Drosophila gene spalt

21 January 2018

1 reference

7 January 2021

spalt encodes an evolutionarily conserved zinc finger protein of novel structure which provides homeotic gene function in the head and tail region of the Drosophila embryo

1 reference

7 January 2021

A gene complex acting downstream of dpp in Drosophila wing morphogenesis.

1 reference

7 January 2021

Two distinct mechanisms for long-range patterning by Decapentaplegic in the Drosophila wing.

1 reference

7 January 2021

Direct and long-range action of a DPP morphogen gradient.

1 reference

7 January 2021

The mouse homolog of the region specific homeotic gene spalt of Drosophila is expressed in the developing nervous system and in mesoderm-derived structures

1 reference

7 January 2021

Xenopus Xsal-1, a vertebrate homolog of the region specific homeotic gene spalt of Drosophila

1 reference

7 January 2021

Hearing loss in Townes-Brocks syndrome

1 reference

7 January 2021

Phenotypic variability in Townes-Brocks syndrome

1 reference

7 January 2021

Townes-Brocks syndrome in two mentally retarded youngsters

1 reference

7 January 2021

Townes-Brocks syndrome associated with mental retardation.

1 reference

7 January 2021

Head and tail development of the Drosophila embryo involves spalt, a novel homeotic gene.

1 reference

7 January 2021

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

1 reference

7 January 2021

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

1 reference

7 January 2021

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

1 reference

7 January 2021

Post-translational processing and renal expression of mouse Indian hedgehog

1 reference

7 January 2021

A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye

1 reference

7 January 2021

BMP-7 is an inducer of nephrogenesis, and is also required for eye development and skeletal patterning

1 reference

7 January 2021