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Clinodactyly
Known as:
Finger clinodactyly
An angulation of a digit at an interphalangeal joint in the plane of the palm (finger) or sole (toe). [pmid:16252026]
National Institutes of Health
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Related topics
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50 relations
AMINOPTERIN SYNDROME SINE AMINOPTERIN
Aarskog syndrome
Blepharo-cheilo-dontic syndrome
Brachydactyly, Type A1, B
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Coexisting Edward syndrome and Klinefelter syndrome
K. P. Weeraesekara
,
A. Sirisena
2013
Corpus ID: 73329311
Sri Lanka Journal of Child Health , 2013; 42 (3): 170-172 (Key words: Double aneuploidy; Edward syndrome; Klinefelter syndrome…
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2003
2003
Mosaicism del(8p)/inv dup(8p) in a dysmorphic female infant: a mosaic formed by a meiotic error at the 8p OR gene and an independent terminal deletion event
J. Vermeesch
,
R. Thoelen
,
I. Salden
,
M. Raes
,
G. Matthijs
,
J. Fryns
Journal of Medical Genetics
2003
Corpus ID: 8112903
Various chromosomal rearrangements are associated with the distal 8p region. Among them are the inv dup(8p),1 del(8p22),2–5 and…
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2002
2002
Pigmentary mosaicism of the hyperpigmented type in two half-brothers.
D. Horn
,
R. Happle
,
H. Neitzel
,
J. Kunze
American journal of medical genetics
2002
Corpus ID: 9985458
Pigmentary mosaicism is a heterogeneous cutaneous phenotype that is often associated with extracutaneous anomalies. It is widely…
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1991
1991
Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome).
A. Watty
,
F. Prieto
,
M. Beneyto
,
M. Neugebauer
,
A. Gal
American journal of medical genetics
1991
Corpus ID: 45659634
A mapping study was performed on a 3-generation Spanish family with X-linked syndromal mental retardation. Affected males have a…
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1987
1987
Interstitial deletion of chromosome 2 (p23p25).
V. Penchaszadeh
,
P. Dowling
,
J. Davis
,
R. Schmidt
,
R. Wapnir
American journal of medical genetics
1987
Corpus ID: 40319278
We report a patient with a de novo interstitial deletion of the short arm of chromosome 2 (p23p25). The patient had microcephaly…
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1985
1985
Partial trisomy 12q24.31----qter.
ELOfZA Helena
,
Tajara
,
+10 authors
Saco Paulo
Journal of Medical Genetics
1985
Corpus ID: 28698141
Clinical details of a male child with the karyotype 46,XY,-4,+der(4),t(4;12) (p16;q24.31)mat are reported and compared with those…
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1981
1981
Keratosis palmaris et plantaris with clinodactyly. A distinct autosomal dominant genodermatosis.
M. Aguirre‐Negrete
,
A. Hernández
,
+4 authors
J. Cantú
Dermatologica
1981
Corpus ID: 34659128
Keratosis palmaris et plantaris and clinodactyly of the 5th finger was diagnosed in 11 members of a family with a typical pattern…
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1979
1979
The Summitt syndrome: observations on a third case.
C. Sells
,
J. Hanson
,
J. Hall
American journal of medical genetics
1979
Corpus ID: 24497093
A 6 1/2 year old male presented with acrocephaly, brachydactyly, clinodactyly, mild syndactyly of the hands and feet, genu valgum…
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1969
1969
Dermatoglyphic defects and rubella teratogenesis.
S. Purvis-Smith
,
P. Howard
,
M. Menser
1969
Corpus ID: 71725369
The dermatoglyphic patterns of 100 children with congenital rubella were studied and compared with those of 100 matched normal…
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Review
1966
Review
1966
The XXXXY chromosome anomaly: report of three new cases and review of 30 cases from the literature.
W. Zaleski
,
C. Houston
,
J. Pozsonyi
,
K. Ying
Canadian Medical Association journal
1966
Corpus ID: 39474058
The majority of abnormal sex chromosome complexes in the male have been considered to be variants of Klinefelter's syndrome but…
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