(Q41930326)

14 October 2017

title

Normal Y sequences in Smith-Lemli-Opitz syndrome with total failure of masculinization (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

Smith-Lemli-Opitz syndrome

21 September 2022

main subject

1 reference

R. Fukazawa

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

Y. Nakahori

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

T. Kogo

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

T. Kawakami

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

H. Akamatsu

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

A. Tanae

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

I. Hibi

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

S. Nagafuchi

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

Y. Nakagome

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

T. Hirayama

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1392379

21 September 2022

language of work or name

English

0 references

publication date

1 June 1992

1 reference

14 October 2017

1 reference

14 October 2017

volume

81

1 reference

14 October 2017

issue

6-7

1 reference

14 October 2017

page(s)

570-572

1 reference

Hirschsprung disease in a 46,XY phenotypic infant girl with Smith-Lemli-Opitz syndrome

14 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1992.TB12300.X

Female external genitalia and müllerian duct derivatives in a 46,XY infant with the smith-lemli-Opitz syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1992.TB12300.X

Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1992.TB12300.X

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1992.TB12300.X

Molecular cloning and mapping of 10 new probes on the human Y chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1992.TB12300.X

The sex-determining region of the human Y chromosome encodes a finger protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1992.TB12300.X

Population structure of the human pseudoautosomal boundary

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1992.TB12300.X

A NEWLY RECOGNIZED SYNDROME OF MULTIPLE CONGENITAL ANOMALIES.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.1992.TB12300.X

10.1111/J.1651-2227.1992.TB12300.X

21 January 2018

Identifiers

DOI

1 reference

14 October 2017

1 reference