(Q28181736)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1347149

16 September 2022

A Milunsky

5

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author name string

C. T. Baldwin

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1347149

16 September 2022

C. F. Hoth

2

1 reference

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16 September 2022

J. A. Amos

3

1 reference

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16 September 2022

E. O. da-Silva

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1347149

Waardenburg I syndrome: a clinical and genetic study of two large Brazilian kindreds, and literature review

16 September 2022

language of work or name

English

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publication date

13 February 1992

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published in

Nature

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volume

355

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page(s)

637-8

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issue

6361

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cites work

1 reference

7 January 2021

Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3).

1 reference

7 January 2021

Mouse and hamster mutants as models for Waardenburg syndromes in humans

1 reference

7 January 2021

DNA binding by proteins

1 reference

7 January 2021

A Genetic Model for Interaction of the Homeodomain Recognition Helix with DNA

1 reference

7 January 2021

splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3

1 reference

7 January 2021

A frame-shift mutation in the cystic fibrosis gene.

1 reference

7 January 2021

Pax-3, a novel murine DNA binding protein expressed during early neurogenesis.

1 reference

7 January 2021

undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1

1 reference

7 January 2021

The molecular basis of the undulated/Pax-1 mutation

1 reference

7 January 2021

Mutations in type I procollagen genes that cause osteogenesis imperfecta

1 reference

7 January 2021

Probing the basic defect in cystic fibrosis

1 reference

7 January 2021

Identification and characterization of the gene for neurofibromatosis type 1.

1 reference

7 January 2021

Observations on the Histogenesis of the Inner Ear Degeneration of the Deaf White Cat and Its Possible Relationship to the Ætiology of Certain Unexplained Varieties of Human Congenital Deafness

1 reference

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

7 January 2021

Dimensions Publication ID

Identifiers

DOI

10.1038/355637A0

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1032292739

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