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Acquired cubitus valgus
Known as:
Cubitus valgus
, Cubitus valgus (acquired)
, Outward turned elbows
Abnormal positioning in which the elbows are turned out. [HPO:probinson]
National Institutes of Health
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Related topics
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20 relations
CAMPTODACTYLY SYNDROME, GUADALAJARA TYPE I
COLD-INDUCED SWEATING SYNDROME 2
Cohen syndrome
Congenital cubitus valgus
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
Partial trisomie 5q: Three different phenotypes depending on different duplication segments
A. Rodewald
,
M. Zankl
,
E. Gley
,
K. Zang
Human Genetics
2004
Corpus ID: 38941462
SummaryOn the basis of phenotypic similarities and differences among patients with a partial trisomy of chromosome 5q, three…
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2002
2002
SHOX nullizygosity and haploinsufficiency in a Japanese family: implication for the development of Turner skeletal features.
T. Ogata
,
K. Muroya
,
G. Sasaki
,
G. Nishimura
,
H. Kitoh
,
T. Hattori
Journal of Clinical Endocrinology and Metabolism
2002
Corpus ID: 25429879
We report on clinical and molecular findings in a Japanese family consisting of a male infant with SHOX nullizygosity and his…
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2001
2001
Growth hormone and gonadotropin-releasing hormone analog therapy in haploinsufficiency of SHOX.
Tsutomu Ogata
,
K. Onigata
,
Tomoyuki Hotsubo
,
N. Matsuo
,
G. A. Rappold
Endocrine journal
2001
Corpus ID: 24678037
We report on GH (0.5 IU or 0.17 mg/kg/week) and GnRH analog (GnRHa, 60 microg/kg, every 4 weeks) therapy in SHOX…
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2000
2000
Cubitus interruptus Requires DrosophilaCREB-Binding Protein To Activate wingless Expression in theDrosophila Embryo
Yang Chen
,
R. Goodman
,
S. Smolik
Molecular and Cellular Biology
2000
Corpus ID: 25880233
ABSTRACT CREB-binding protein (CBP) serves as a transcriptional coactivator in multiple signal transduction pathways. The…
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2000
2000
Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features
M. Adachi
,
K. Tachibana
,
Y. Asakura
,
K. Muroya
,
T. Ogata
Human Genetics
2000
Corpus ID: 11472383
Abstract. We report a mother and two daughters with partial Xp monosomy. Clinical assessment for Turner phenotype revealed that…
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1998
1998
Noonan syndrome associated with central giant cell granuloma
B. Uçar
,
A. Ökten
,
H. Mocan
,
C. Erçin
Clinical Genetics
1998
Corpus ID: 35556892
We report a case of Noonan syndrome associated with central giant cell granuloma. The patient was a 101/2‐year‐old boy with the…
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1974
1974
The carrying angle in sex chromosome anomalies.
F. Baughman
,
J. Higgins
,
T. Wadsworth
,
M. Demaray
Journal of the American Medical Association (JAMA…
1974
Corpus ID: 29003565
The carrying angle is said to be greater in the XO phenotype than in XX and greater in XX than in XY. To determine the effects of…
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1968
1968
Middle ear disease in Turner's syndrome.
J. Szpunar
,
M. Rybak
A M A Archives of Otolaryngology
1968
Corpus ID: 40353701
IN 1938 HENRY TURNER 1 reported a syndrome consisting of shortness of stature, sexual underdevelopment, short, "webbed" neck, and…
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Review
1966
Review
1966
Eye signs in Turner's syndrome.
S. Lessell
,
A. Forbes
A M A Archives of Ophthalmology
1966
Corpus ID: 5906619
Chromosome analyses have revealed consistent abnormalities in several congenital disorders. Two of these, mongolism (21 trisomy…
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1964
1964
A VERY LARGE METACENTRIC CHROMOSOME IN A WOMAN WITH SYMPTOMS OF TURNER'S SYNDROME.
Gouw Wie Lie
,
J. Coenegracht
,
G. Stalder
Cytogenetics
1964
Corpus ID: 43160668
A sex chromatin positive woman has stunted growth, primary amenor-rhoea, cubitus valgus, Madelung’s deformity and mental…
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