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20p12
A chromosome band present on 20p
National Institutes of Health
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Related topics
Related topics
3 relations
BMP2 wt Allele
Chromosome 20 Short Arm
Chromosomes
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Mckusick Kaufman Syndrome Accompanied by Congenital Laryngomalacia , Intestinal Malrotation and Hypothalamic Hamartom
I. Ciftci
,
A. Annagür
,
E. Uysal
,
M. Sivri
,
C. Erol
,
A. Taştekin
2014
Corpus ID: 11530536
McKusick-Kaufman syndrome is a rare syndrome inherited in an autosomal recessive pattern with a phenotypic triad comprising…
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Review
2012
Review
2012
Manifestaciones dermatológicas del síndrome de Alagille
André Morales Martínez
,
C. A. M. Cedillos
,
J. N. Zermeño
,
Verónica Fabiola Morán Barroso
,
S. V. Carrión
,
Silvia Marinne Ramírez Dovala
2012
Corpus ID: 71040339
Alagille syndrome (MIM #118450) causes the majority of cases of congenital cholestasis. It is an autosomal dominant multisystem…
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Review
2003
Review
2003
Alagille-syndroom: klinische en genetische aspecten
C. Marcelis
,
P. Forget
,
U. Moog
2003
Corpus ID: 71897234
SummaryAlagille syndrome (ags, omim *118450) is an autosomal dominant disease that involves liver, heart, eyes, skeleton and…
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1998
1998
Primary Sjögren ’ s syndrome and aplastic anaemia
1998
Corpus ID: 262018453
Primary Sjögren’s syndrome (SS) is an autoimmune disease characterised by the presence of xerostomia and xerophthalmia without…
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1998
1998
Primary Sjögren ’ s syndrome and aplastic anaemia
1998
Corpus ID: 262018442
Primary Sjögren’s syndrome (SS) is an autoimmune disease characterised by the presence of xerostomia and xerophthalmia without…
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1998
1998
Primary Sjögren ’ s syndrome and aplastic anaemia
1998
Corpus ID: 262018445
Primary Sjögren’s syndrome (SS) is an autoimmune disease characterised by the presence of xerostomia and xerophthalmia without…
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1998
1998
Primary Sjögren ’ s syndrome and aplastic anaemia
I. Quiquandon
,
Pierre Morel
,
+5 authors
Cimmino Recently
1998
Corpus ID: 262018430
Primary Sjögren’s syndrome (SS) is an autoimmune disease characterised by the presence of xerostomia and xerophthalmia without…
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1996
1996
Etude genetique du syndrome d'alagille et cartographie physique d'un locus correspondant en 20p12
Sophie Dhorne-Pollet
1996
Corpus ID: 159691741
Le syndrome d'alagille (ags, mim 118450) est un syndrome malformatif complexe caracterise par l'association de cinq elements…
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1987
1987
Localization and linkage of three polymorphic DNA sequences on human chromosome 20.
P. Goodfellow
,
Alessandra M. V. Duncan
,
+5 authors
N. Simpson
Cytogenetics and Cell Genetics
1987
Corpus ID: 19083639
The D20S6 locus has been sublocalized by in situ hybridization using the pD3H12 probe to human chromosome band 20p12 and the…
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1985
1985
Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.
P. Goodfellow
,
B. N. White
,
+6 authors
N. Simpson
American Journal of Human Genetics
1985
Corpus ID: 9383484
A DNA segment D20S5 isolated from a chromosome 19/20 flow-sorted library was shown to identify two restriction fragment length…
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