(Q68929823)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3543368%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

review article

1 reference

title

Noonan syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3543368%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

1 reference

J E Allanson

1 reference

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28 September 2019

publication date

1 January 1987

1 reference

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Journal of Medical Genetics

28 September 2019

published in

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28 September 2019

volume

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28 September 2019

issue

1 reference

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28 September 2019

page(s)

9-13

1 reference

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Keratosis pilaris atrophicans faciei (Ulerythema ophryogenes): a cutaneous marker in the Noonan syndrome

28 September 2019

cites work

1 reference

12 December 2020

The orthopedic aspects of the fetal alcohol syndrome

1 reference

12 December 2020

Noonan's syndrome. IQ and specific disabilities

1 reference

12 December 2020

Noonan phenotype with polydactyly

1 reference

12 December 2020

Familial Williams syndrome

1 reference

12 December 2020

Malignant hyperthermia associated with myopathy and normal muscle enzymes

1 reference

12 December 2020

Growth and pubertal development in five boys with Noonan's syndrome

1 reference

12 December 2020

Postoperative hyperpyrexia in a case of Noonan's syndrome.

1 reference

12 December 2020

Ullrich-Turner syndrome in the male: review of the literature and report of a case with lymphocytic (Hashimoto's) thyroiditis

1 reference

12 December 2020

Chiari (type 1) malformation and syringomyelia in a patient with Noonan's syndrome

1 reference

12 December 2020

Multiple odontogenic keratocysts in a case of the Noonan syndrome

1 reference

12 December 2020

Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome

1 reference

12 December 2020

1 reference

12 December 2020

Neck web and congenital heart defects: a pathogenic association in 45 X-O Turner syndrome?

1 reference

12 December 2020

Noonan phenotype associated with neurofibromatosis

1 reference

12 December 2020

A distinctive facial appearance in neurofibromatosis von Recklinghausen

1 reference

12 December 2020

The neurofibromatosis-Noonan syndrome

1 reference

12 December 2020

Noonan syndrome in a patient with hyperplasia of the myenteric plexuses and neurofibromatosis

1 reference

12 December 2020

Noonan syndrome: a review

1 reference

12 December 2020

The Ullrich-Noonan syndrome (Turner phenotype).

1 reference

12 December 2020

Anesthetic-induced malignant hyperpyrexia in children.

1 reference

12 December 2020

Noonan's syndrome and autoimmune thyroiditis.

1 reference

12 December 2020

Arthrogryposis Multiplex Congenita and the Turner Phenotype

1 reference

12 December 2020

Trimethylaminuria: the fish-odour syndrome

1 reference

12 December 2020

Pheochromocytoma and hyporesponsiveness to thyrotrophin in a 46 XY male with features of the Turner phenotype

1 reference

12 December 2020

Noonan's syndrome. A case with elevated serum alkaline phosphatase levels and malignant schwannoma of the left forearm

1 reference

12 December 2020

Turner's syndrome in a male. Report of a case with myopia, retinal detachment, cataract, and glaucoma

1 reference

12 December 2020

Aarskog syndrome. New findings and genetic analysis

1 reference

12 December 2020

Congenital hypoplastic anemia terminating in acute promyelocytic leukemia

1 reference

12 December 2020

Noonan syndrome: the changing phenotype

1 reference

12 December 2020

Cardiovascular anomalies in Noonan's syndrome

1 reference

12 December 2020

Noonan syndrome-an unusual family with above average intelligence, a high incidence of cancer and rare type of vasculitis

1 reference

12 December 2020

Possible etiologic mechanisms of the short stature in the Noonan syndrome

1 reference

12 December 2020

Congenital stem cell dysfunction associated with Turner-like phenotype

1 reference

12 December 2020

An evaluation of the possible association of malignant hyperpyrexia with the Noonan syndrome using serum creatine phosphokinase levels

1 reference

12 December 2020

Teratogenic effects associated with maternal primidone therapy

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.24.1.9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3543368%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3543368%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

PubMed publication ID

3543368

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3543368%20AND%20SRC:MED&resulttype=core&format=json