(Q33538409)

27 July 2017

1 reference

title

Kenny-Caffey syndrome: an Arab variant? (English)

1 reference

27 July 2017

Kenny-Caffey syndrome

1 reference

Sabry MA

1

1 reference

27 July 2017

Farag TI

2

1 reference

27 July 2017

Shaltout AA

3

1 reference

27 July 2017

Zaki M

4

1 reference

27 July 2017

Al-Mazidi Z

5

1 reference

27 July 2017

Abulhassan SJ

6

1 reference

27 July 2017

Al-Torki N

7

1 reference

27 July 2017

Quishawi A

8

1 reference

27 July 2017

Al Awadi SA

9

1 reference

27 July 2017

1 January 1999

1 reference

27 July 2017

1 reference

27 July 2017

55

1 reference

27 July 2017

1

1 reference

27 July 2017

44-49

1 reference

Correlation of urethral resistance and shape in girls

27 July 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

The Kenny-Caffey syndrome: Growth retardation and hypocalcemia in a young boy

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

Kenny syndrome: evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in one.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

Congenital medullary tubular stenosis. A case of Caffey-Kenny syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

Kenny syndrome: description of additional abnormalities and molecular studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

Kenny–Caffey syndrome in two sibs born to consanguineous parents: Evidence for an autosomal recessive variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

Short stature, mental retardation, and hypoparathyroidism: a new syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

Syndrome of hypoparathyroidism, growth hormone deficiency, and multiple minor anomalies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

DiGeorge syndrome: part of CATCH 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

Congenital stenosis of medullary spaces in tubular bones and calvaria in two proportionate dwarfs--mother and son; coupled with transitory hypocalcemic tetany

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

7 January 2021

The Kenny syndrome, a rare type of growth deficiency with tubular stenosis, transient hypoparathyroidism and anomalies of refraction

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

7 January 2021

Congenital hypoparathyroidism, seizure, extreme growth failure with developmental delay and dysmorphic features--another case of this new syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

7 January 2021

Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

7 January 2021

Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.550108.X

7 January 2021

10.1034/J.1399-0004.1999.550108.X

Identifiers

DOI

1 reference

27 July 2017

1 reference