-
Keratosis pilaris atrophicans faciei (ulerythema ophryogenes): a cutaneous marker in the Noonan syndrome.
Br J Dermatol. 1979 Apr;100(4):409-16
PMID: 454568
-
The orthopedic aspects of the fetal alcohol syndrome.
Clin Orthop Relat Res. 1979 Mar-Apr;(139):58-63
PMID: 455851
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Noonan's syndrome. IQ and specific disabilities.
Am J Dis Child. 1979 Aug;133(8):846-50
PMID: 463839
-
Noonan phenotype with polydactyly.
Birth Defects Orig Artic Ser. 1979;15(5B):313-9
PMID: 526585
-
Familial Williams syndrome.
Clin Genet. 1980 Sep;18(3):173-6
PMID: 7192194
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Malignant hyperthermia associated with myopathy and normal muscle enzymes.
J Pediatr. 1977 Sep;91(3):431-4
PMID: 894412
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Growth and pubertal development in five boys with Noonan's syndrome.
Arch Dis Child. 1982 Jan;57(1):13-7
PMID: 6121534
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Postoperative hyperpyrexia in a case of Noonan's syndrome.
Indian Heart J. 1982 May-Jun;34(3):180-2
PMID: 7129500
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Ullrich-Turner syndrome in the male: review of the literature and report of a case with lymphocytic (Hashimoto's) thyroiditis.
Mayo Clin Proc. 1966 Dec;41(12):843-54
PMID: 5953597
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Chiari (type 1) malformation and syringomyelia in a patient with Noonan's syndrome.
J Neurol Neurosurg Psychiatry. 1982 Aug;45(8):753-4
PMID: 7131003
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Multiple odontogenic keratocysts in a case of the Noonan syndrome.
Br J Oral Surg. 1982 Sep;20(3):213-6
PMID: 6958319
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Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome.
J Pediatr. 1983 Feb;102(2):224-7
PMID: 6822926
-
The Noonan syndrome.
Eur Heart J. 1983 Apr;4(4):223-9
PMID: 6884370
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Neck web and congenital heart defects: a pathogenic association in 45 X-O Turner syndrome?
Teratology. 1984 Jun;29(3):355-61
PMID: 6463900
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Noonan phenotype associated with neurofibromatosis.
Am J Med Genet. 1985 Jul;21(3):457-62
PMID: 2411134
-
A distinctive facial appearance in neurofibromatosis von Recklinghausen.
Am J Med Genet. 1985 Jul;21(3):463-70
PMID: 3927724
-
The neurofibromatosis-Noonan syndrome.
Am J Med Genet. 1985 Jul;21(3):471-6
PMID: 3927725
-
Noonan syndrome in a patient with hyperplasia of the myenteric plexuses and neurofibromatosis.
Am J Med Genet. 1985 Jul;21(3):491-2
PMID: 3927727
-
Noonan syndrome: a review.
Am J Med Genet. 1985 Jul;21(3):493-506
PMID: 3895929
-
The Ullrich-Noonan syndrome (Turner phenotype).
Am J Dis Child. 1974 Jan;127(1):48-55
PMID: 4809794
-
Anesthetic-induced malignant hyperpyrexia in children.
J Pediatr. 1973 Jul;83(1):37-40
PMID: 4149045
-
Noonan's syndrome and autoimmune thyroiditis.
J Pediatr. 1973 Aug;83(2):237-40
PMID: 4123925
-
Arthrogryposis multiplex congenita and the Turner phenotype.
Am J Dis Child. 1972 Feb;123(2):141-4
PMID: 5025860
-
Trimethylaminuria: the fish-odour syndrome.
Lancet. 1970 Oct 10;2(7676):770-1
PMID: 4195988
-
Pheochromocytoma and hyporesponsiveness to thyrotrophin in a 46 XY male with features of the Turner phenotype.
Ann Intern Med. 1969 Feb;70(2):325-33
PMID: 5764508
-
Noonan's syndrome. A case with elevated serum alkaline phosphatase levels and malignant schwannoma of the left forearm.
Am J Dis Child. 1968 Oct;116(4):359-66
PMID: 5697968
-
Turner's syndrome in a male. Report of a case with myopia, retinal detachment, cataract, and glaucoma.
Arch Ophthalmol. 1967 May;77(5):630-4
PMID: 6022732
-
Aarskog syndrome. New findings and genetic analysis.
JAMA. 1978 Dec 8;240(24):2638-41
PMID: 712980
-
Congenital hypoplastic anemia terminating in acute promyelocytic leukemia.
Pediatrics. 1978 Jun;61(6):898-901
PMID: 276838
-
Noonan syndrome: the changing phenotype.
Am J Med Genet. 1985 Jul;21(3):507-14
PMID: 4025385
-
Cardiovascular anomalies in Noonan's syndrome.
Chest. 1977 May;71(5):677-9
PMID: 852354
-
Noonan syndrome-an unusual family with above average intelligence, a high incidence of cancer and rare type of vasculitis.
Birth Defects Orig Artic Ser. 1976;12(1):181-6
PMID: 990443
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Possible etiologic mechanisms of the short stature in the Noonan syndrome.
Birth Defects Orig Artic Ser. 1976;12(6):127-33
PMID: 974248
-
Congenital stem cell dysfunction associated with Turner-like phenotype.
J Pediatr. 1976 Jun;88(6):979-82
PMID: 1271198
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An evaluation of the possible association of malignant hyperpyrexia with the Noonan syndrome using serum creatine phosphokinase levels.
J Pediatr. 1975 Mar;86(3):412-5
PMID: 1113229
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Teratogenic effects associated with maternal primidone therapy.
J Pediatr. 1981 Jul;99(1):160-2
PMID: 7252656