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The genodermatoses and their significance in pediatric dermatology.
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Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
review article
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Europe PubMed Central
title
The genodermatoses and their significance in pediatric dermatology
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
author name string
Alper JC
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
publication date
1 January 1986
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
published in
Dermatologic Clinics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
volume
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
page(s)
45-54
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
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7 January 2021
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Birthmarks with serious medical significance: Nevocellular nevi, sebaceous nevi, and multiple café au lait spots
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7 January 2021
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Leaf-shaped lesions of ocular fundus and white eyelashes in tuberous sclerosis
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7 January 2021
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https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
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Alopecia Areata and Down Syndrome
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7 January 2021
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Defective Repair Replication of DNA in Xeroderma Pigmentosum
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7 January 2021
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Rapid complementation method for classifying excision repair-defective xeroderma pigmentosum cell strains
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7 January 2021
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Differences in patterns of complementation of the more common groups of xeroderma pigmentosum: possible implications
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7 January 2021
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Tuberous sclerosis, early onset of seizures, and mental subnormality: study of discordant homozygous twins
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7 January 2021
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Incontinentia Pigmenti: Clinical and Genetical Studies of two Familial Cases
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Crossref
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7 January 2021
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Incontinentia pigmenti achromians
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
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Incontinentia pigmenti: a systemic genodermatosis with striking cutaneous findings
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
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inferred from DOI database lookup
Abnormal DNA histograms of stroma cells in patients with tuberous sclerosis. A cytofluorometric study
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7 January 2021
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Congenital Circumscribed Hypomelanosis: A Characterization Based on Electron Microscopic Study of Tuberous Sclerosis, Nevus Depigmentosus, and Piebaldism
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7 January 2021
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Defective thymine dimer excision from xeroderma pigmentosum chromatin and its characteristic catalysis by cell-free extracts.
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A clinicopathologic study of the skin in mongolism
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7 January 2021
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Von Recklinghausen neurofibromatosis. Incidence of iris hamartomata
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7 January 2021
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Depigmented hair. The earliest sign of tuberous sclerosis
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7 January 2021
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Tuberous sclerosis: a review for the neurosurgeon
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7 January 2021
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Chronic renal failure in patients with tuberous sclerosis. Association with renal cysts
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7 January 2021
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inferred from DOI database lookup
Incontinentia pigmenti achromians (Ito's hypomelanosis).
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Neurocutaneous syndromes
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal diagnosis of xeroderma pigmentosum. Report of the first successful case
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Neurofibromatosis: clinical heterogeneity
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Von Recklinghausen neurofibromatosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
The pathophysiology of neurofibromatosis: IX. Paternal age as a factor in the origin of new mutations.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Xeroderma pigmentosum. An inherited diseases with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Incontinentia pigmenti achromians. Multiple cases within a family
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
The Connective Tissue Nevus-Osteopoikilosis Syndrome
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hypomelanosis of Ito (incontinentia pigmenti achromians): a neurocutaneous syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Early diagnosis, genetic marker sought for tuberous sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Incontinentia pigmenti achromians (Ito)
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Rhabdomyomas of heart: a report of four cases
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Crossref
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https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Thyroid auto-immune disease and thyroid function in families of subjects with Down's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked dominant inherited diseases with lethality in hemizygous males
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic value of the café-au-lait spot in children
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dermatologic manifestations of mongolism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8635%2818%2930843-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0733-8635(18)30843-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
PubMed publication ID
2941201
1 reference
stated in
Europe PubMed Central
PubMed publication ID
2941201
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2941201%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 October 2019
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