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POLYDACTYLY, POSTAXIAL
Known as:
Postaxial hexadactyly
, Postaxial polydactyly
A form of polydactyly in which the extra digit or digits are localized on the side of the fifth finger or fifth toe. [HPO:probinson]
National Institutes of Health
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Related topics
Related topics
50 relations
AU-KLINE SYNDROME
Acrocephalopolysyndactyly type 2
Arima syndrome
Asphyxiating Thoracic Dystrophy 2
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Broader (3)
Fingers
Polydactyly
Toes
Narrower (3)
Polydactyly, Postaxial, Type A1
Postaxial polydactyly type A
Ulnar polydactyly of fingers
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2004
Highly Cited
2004
Bmp4 in limb bud mesoderm regulates digit pattern by controlling AER development.
J. Selever
,
Wei Liu
,
Mei-Fang Lu
,
R. Behringer
,
James F. Martin
Developmental Biology
2004
Corpus ID: 10971258
Highly Cited
2001
Highly Cited
2001
Mutations in MKKS cause Bardet-Biedl syndrome
A. Slavotinek
,
E. Stone
,
+7 authors
L. Biesecker
Nature Genetics
2001
Corpus ID: 1900916
A.M.Slavotinek et al.Nature Genet. 26, 15–16 (2001). Two recent reports1,2 describing mutations in the gene for McKusick-Kaufman…
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Highly Cited
1999
Highly Cited
1999
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.
U. Radhakrishna
,
D. Bornholdt
,
+10 authors
S. Antonarakis
American Journal of Human Genetics
1999
Corpus ID: 24218893
Functional characterization of a gene often requires the discovery of the full spectrum of its associated phenotypes. Mutations…
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Review
1998
Review
1998
Human developmental disorders and the Sonic hedgehog pathway.
J. Ming
,
E. Roessler
,
M. Muenke
Molecular medicine today
1998
Corpus ID: 35575129
Highly Cited
1998
Highly Cited
1998
Prx1 and Prx2 in skeletogenesis: roles in the craniofacial region, inner ear and limbs.
D. T. Berge
,
A. Brouwer
,
J. Korving
,
James F. Martin
,
F. Meijlink
Development
1998
Corpus ID: 40081671
Prx1 and Prx2 are closely related paired-class homeobox genes that are expressed in very similar patterns predominantly in…
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Highly Cited
1997
Highly Cited
1997
Diagnosis of the Meckel-Gruber syndrome at eleven to fourteen weeks' gestation.
Waldo Sepulveda
,
N. Sebire
,
A. Souka
,
R. Snijders
,
K. Nicolaides
American Journal of Obstetrics and Gynecology
1997
Corpus ID: 11449687
Highly Cited
1992
Highly Cited
1992
Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21.
R. Hughes-Benzie
,
A. Hunter
,
J. Allanson
,
Alex Mackenzie
American journal of medical genetics
1992
Corpus ID: 27824687
We report 6 affected males in a 5-generation family with x-linked Simpson-Golabi-Behmel (SGB) syndrome. All had pre- and…
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Highly Cited
1980
Highly Cited
1980
Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly--a new syndrome? Part I: clinical, causal, and pathogenetic considerations.
J. Hall
,
Pallister Pd
,
+7 authors
John M. Optiz
American journal of medical genetics
1980
Corpus ID: 36340128
We report on six infants with a neonatally lethal malformation syndrome of hypothalamic hamartoblastoma, postaxial polydactyly…
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Highly Cited
1980
Highly Cited
1980
Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly--a new syndrome? Part II: Neuropathological considerations.
S. Clarren
,
Ellsworth C. Alvord
,
Judith G. Hall
,
John M. Optiz
American journal of medical genetics
1980
Corpus ID: 24505599
Unusual and virtually identical hypothalamic tumors were recently studied in three unrelated neonates with a similar complex…
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Highly Cited
1978
Highly Cited
1978
A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs.
A. Schinzel
,
A. Giedion
American journal of medical genetics
1978
Corpus ID: 34921784
A brother and sister presented with an uncommon malformation syndrome consisting of severe midface hypoplasia, congenital heart…
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