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Abnormality of the nares
Known as:
Malformation of the nares
, Abnormality of the nostrils
, Malformation of the nostrils
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Abnormality of the nostril. [HPO:curators]
National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Pitt–Hopkins Syndrome and Differential Diagnosis: A Molecular and Clinical Challenge
G. Marangi
,
M. Zollino
Journal of Pediatric Genetics
2015
Corpus ID: 1735523
Abstract Pitt–Hopkins syndrome is an emerging neurodevelopmental disorder caused by haploinsufficiency of the TCF4 gene on…
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2014
2014
A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndrome
A. Kumakura
,
Satoru Takahashi
,
K. Okajima
,
Daisuke Hata
Brain & development (Tokyo. )
2014
Corpus ID: 647275
2014
2014
A construção de identidades: da leitura para o roteiro e do roteiro para a leitura - um estudo analítico de projetos de adaptação de textos literários para jogos digitais
W. S. Araújo
2014
Corpus ID: 191550065
Os roteiros para jogos digitais possuem caracteristicas que devem ser tra-tadas de modo a assegurar o desenvolvimento de…
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2007
2007
Two siblings with an unusual nasal malformation: Further instances of craniorhiny?
M. Lees
,
L. Kangesu
,
Per Hall
,
R. Hennekam
American Journal of Medical Genetics. Part A
2007
Corpus ID: 39909975
We report a brother and sister born to consanguineous parents. The siblings have hypertelorism, bifid nose, upturned nares…
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2005
2005
Robinow Syndrome: a case report.
H. Gulcan
,
A. Akıncı
,
A. Aktar
Genetic Counseling
2005
Corpus ID: 37022572
We report a case with Robinow syndrome which has been rarely reported in the literature. A male newborn who had fetal face…
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2005
2005
TO JMG Deletion 9 q 34 . 3 syndrome : genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly
S. Yatsenko
,
S. Cheung
,
+9 authors
J. Lupski
2005
Corpus ID: 4220
S ubmicroscopic deletion del(9)(q34.3) is a rare constitutional microdeletion syndrome involving the gene-rich subtelomeric…
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Review
2004
Review
2004
Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
S. Chantot-Bastaraud
,
C. Muti
,
+5 authors
B. Simon‐Bouy
Annales de Genetique
2004
Corpus ID: 23018929
Review
2002
Review
2002
Enteral feedings with comfort and safety.
D. Arbogast
Clinical Journal of Oncology Nursing
2002
Corpus ID: 29604230
Patients who are unable to eat by mouth can be fed in a manner that maintains the structural and functional integrity of the…
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1998
1998
Unknown syndrome: peculiar face, severe hypodontia of permanent teeth, and precocious choroid calcifications.
Rosanna Pallotta
,
P. Fusilli
Journal of Medical Genetics
1998
Corpus ID: 20972581
We describe a mother and her twin daughters affected with severe hypodontia of the permanent teeth, precocious calcification of…
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1975
1975
Alar base resection for wide flaring nostrils.
A. Ship
British Journal of Plastic Surgery
1975
Corpus ID: 42962976
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