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Peromelia
The distal parts of the limbs are missing leading to a stump formation. [HPO:probinson]
National Institutes of Health
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Semantic Scholar uses AI to extract papers important to this topic.
1997
1997
A retrospective study of the inheritance of peromelia in Angora goats.
J. Agerholm
,
M. E. Kielsgaard
,
J. Pedersen
,
S. Kobberoe
Zentralblatt für Veterinärmedizin Reihe A
1997
Corpus ID: 39122803
Peromelia, agenesia of the distal parts of the limbs, has been reported as a congenital defect in several animal species. In…
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1994
1994
[Congenital absence of the pectoral muscle with contralateral peromelia of the forearm].
P. Fehlow
,
F. Walther
Klinische Pädiatrie
1994
Corpus ID: 37272953
Report of an imbecile female aged 20 years with congenital absence of the pectoral muscle (abortive Poland anomaly) at the right…
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1992
1992
Hereditary peromelia in Mohair goats.
J. S. Nielsen
,
J. Arnbjerg
Zentralblatt für Veterinärmedizin Reihe A
1992
Corpus ID: 20773428
The occurrence of a new congenital defect of the appendicular skeleton in Mohair goats is described. The malformation is…
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Review
1988
Review
1988
Splenic gonadal fusion.
M. Walther
,
T. S. Trulock
,
D. Finnerty
,
J. Woodard
Urology
1988
Corpus ID: 32411571
Review
1985
Review
1985
The spectrum of splenogonadal fusion
A. Gouw
,
J. Elema
,
Mte Binkboelkens
,
H. Dejongh
,
L. Tenkate
European Journal of Pediatrics
1985
Corpus ID: 9339886
Splenogonadal fusion is a rare congenital malformation in which there is an abnormal fusion between the spleen and the gonad or…
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1982
1982
Unusual cardiac malformations in splenogonadal fusion-peromelia syndrome: relationship to normal development.
K. Loomis
,
G. Moore
,
G. Hutchins
Teratology
1982
Corpus ID: 40761708
A male newborn infant, studied at autopsy, showed continuous splenogonadal fusion and severe peromelia associated with an unusual…
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Review
1976
Review
1976
Studies of malformation syndromes of man XXXXI B: Nosologic studies in the Hanhart and the Möbius syndrome
J. Herrmann
,
Pallister Pd
,
+4 authors
J. Opitz
European Journal of Pediatrics
1976
Corpus ID: 23498856
We reviewed etiologic and phenotypic aspects of those orofacial and limb anomalies usually diagnosed as Hanhart syndrome and M…
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Highly Cited
1975
Highly Cited
1975
Splenogonadal fusion-a rare congenital anomaly demonstrated by 99Tc-sulfur colloid imaging: case report.
U. Guarin
,
Z. Dimitrieva
,
S. Ashley
Journal of Nuclear Medicine
1975
Corpus ID: 20222016
A case report illustrating the value of spleen scanning in the diagnosis of a rare anomaly characterized by fusion of the spleen…
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1969
1969
Micrognathia, an associated defect of Hanhart's syndrome, Types II and III
L. Garner
,
D. Bixler
1969
Corpus ID: 72315535
1968
1968
Aglossia-adactylia syndrome.
E. Kelln
,
C. Bennett
,
W. G. Klingberg
A M A Journal of Diseases of Children
1968
Corpus ID: 6784976
EARLY reports, related findings, and an excellent bibliography of the rare aglossia-adactylia syndrome have been published.1There…
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