(Q43548789)

24 November 2017

title

Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLIN. (English)

1 reference

Cenani-Lenz syndactyly syndrome

24 November 2017

1 reference

1 reference

Bacchelli C

1

1 reference

24 November 2017

Goodman FR

series ordinal

2

1 reference

24 November 2017

Scambler PJ

series ordinal

3

1 reference

24 November 2017

Winter RM

series ordinal

4

1 reference

24 November 2017

publication date

1 March 2001

1 reference

24 November 2017

1 reference

24 November 2017

volume

59

1 reference

24 November 2017

issue

3

1 reference

24 November 2017

page(s)

203-205

1 reference

Oligodactyly and multiple synostoses of the extremities: two cases in sibs. A variant of Cenani-Lenz syndactyly

24 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

Dermatoglyphics in patients with Cenani-Lenz type syndactyly: studies in a new case

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

An inherited limb deformity created by insertional mutagenesis in a transgenic mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

Deficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (ld) mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

'Formins': proteins deduced from the alternative transcripts of the limb deformity gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

Formin defines a large family of morphoregulatory genes and functions in establishment of the polarising region

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

Signal relay by BMP antagonism controls the SHH/FGF4 feedback loop in vertebrate limb buds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

DRM/GREMLIN (CKTSF1B1) maps to human chromosome 15 and is highly expressed in adult and fetal brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

Split-hand and split-foot deformity inherited as an autosomal recessive trait

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Present nosology of the Cenani-Lenz type of syndactyly

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Co-segregation of an apparently balanced reciprocal t(12;22)(p11.2;q13.3) with a complex type of 3/3'/4 synpolydactyly associated with metacarpal, metatarsal and tarsal synostoses in three family members

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590312.X

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1034/J.1399-0004.2001.590312.X

1 reference

24 November 2017

1 reference