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Results 1 - 20 of 3,874  for All Library Resources

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Refined by: creation date: 1993 To 2007 remove
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1
Photogenodermatoses: The red face
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Article
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Photogenodermatoses: The red face

Clinics in dermatology, 1993, Vol.11 (2), p.275-281 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0738-081X ;EISSN: 1879-1131

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2
Fetal Alcohol Syndrome and Alcohol Related Birth Defects: Implications and Assurance for Quality of Life
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Article
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Fetal Alcohol Syndrome and Alcohol Related Birth Defects: Implications and Assurance for Quality of Life

B.C. journal of special education, 1993, Vol.17 (3), p.261 [Peer Reviewed Journal]

ISSN: 0704-7509

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3
A recurrent delation in the KIT (mast/stem cell growth factor receptor) proto-oncogene is a frequent cause of human piebaldism
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Article
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A recurrent delation in the KIT (mast/stem cell growth factor receptor) proto-oncogene is a frequent cause of human piebaldism

Human molecular genetics, 1993, Vol.2 (9), p.1499-1500 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0964-6906 ;EISSN: 1460-2083

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4
Bart syndrome
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Article
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Bart syndrome

Indian journal of dermatology, venereology, and leprology, 1993, Vol.59 (3), p.151-153

1994 INIST-CNRS ;ISSN: 0378-6323 ;EISSN: 0973-3922 ;CODEN: IJDLDY

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5
The Nägeli-Franceschetti-Jadassohn Syndrome: A Hereditary Ectodermal Defect Leading to Colloid-Amyloid Formation in the Dermis
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Article
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The Nägeli-Franceschetti-Jadassohn Syndrome: A Hereditary Ectodermal Defect Leading to Colloid-Amyloid Formation in the Dermis

Dermatology (Basel), 1993, Vol.187 (3), p.169-173 [Peer Reviewed Journal]

1993 S. Karger AG, Basel ;1993 INIST-CNRS ;ISSN: 1018-8665 ;EISSN: 1421-9832 ;DOI: 10.1159/000247236 ;PMID: 8219417

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6
Giant hemangioma of the parotid gland associated with Kasabach-Merritt syndrome
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Article
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Giant hemangioma of the parotid gland associated with Kasabach-Merritt syndrome

Journal of oral and maxillofacial surgery, 1993, Vol.51 (4), p.425-428 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0278-2391 ;EISSN: 1531-5053 ;CODEN: JOMSDA

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7
Adams-Oliver Syndrome: Cutis marmorata teleangiectatica congenita with Multiple Anomalies
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Article
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Adams-Oliver Syndrome: Cutis marmorata teleangiectatica congenita with Multiple Anomalies

Dermatology (Basel), 1993, Vol.187 (3), p.205-208 [Peer Reviewed Journal]

1993 S. Karger AG, Basel ;1993 INIST-CNRS ;ISSN: 1018-8665 ;EISSN: 1421-9832 ;DOI: 10.1159/000247244 ;PMID: 8219425

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8
A large duplication in the gene for lysil hydroxylase accounts for the type VI variant of Ehlers-Danlos syndrome in two siblings
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Article
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A large duplication in the gene for lysil hydroxylase accounts for the type VI variant of Ehlers-Danlos syndrome in two siblings

Genomics (San Diego, Calif.), 1993, Vol.15 (2), p.399-404 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0888-7543 ;EISSN: 1089-8646

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9
Mast Cell Abnormalities in the Chédiak-Higashi Syndrome
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Article
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Mast Cell Abnormalities in the Chédiak-Higashi Syndrome

International archives of allergy and immunology, 1993, Vol.100 (2), p.89-92 [Peer Reviewed Journal]

1993 S. Karger AG, Basel ;1993 INIST-CNRS ;ISSN: 1018-2438 ;EISSN: 1423-0097 ;DOI: 10.1159/000236393 ;PMID: 7680257

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10
Complementation of DNA repair defect in xeroderma pigmentosum cells of group C by the transfer of human chromosome 5
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Article
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Complementation of DNA repair defect in xeroderma pigmentosum cells of group C by the transfer of human chromosome 5

Somatic cell and molecular genetics, 1993, Vol.19 (1), p.83-93 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0740-7750 ;EISSN: 1572-9931 ;DOI: 10.1007/BF01233957 ;PMID: 8460401 ;CODEN: SCMGDN

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11
A case of xerodermal pigmentosum complementation group F with neurological abnormalities
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Article
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A case of xerodermal pigmentosum complementation group F with neurological abnormalities

British journal of dermatology (1951), 1993, Vol.128 (1), p.91-94 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0007-0963 ;EISSN: 1365-2133 ;CODEN: BJDEAZ

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12
Sclerotic bone lesions in Gorlin's syndrome
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Article
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Sclerotic bone lesions in Gorlin's syndrome

British journal of radiology, 1993, Vol.66 (781), p.77-80 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0007-1285 ;EISSN: 1748-880X ;DOI: 10.1259/0007-1285-66-781-77 ;PMID: 8428256 ;CODEN: BJRAAP

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13
Buschke-Ollendorff syndrome
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Article
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Buschke-Ollendorff syndrome

Pediatric dermatology, 1993, Vol.10 (1), p.85-87 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0736-8046 ;EISSN: 1525-1470 ;CODEN: PEDRDQ

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14
Tyrosinase gene mutations causing oculocutaneous albinisms: Molecular and biological control of melanogenesis and melanoma
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Article
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Tyrosinase gene mutations causing oculocutaneous albinisms: Molecular and biological control of melanogenesis and melanoma

Journal of investigative dermatology, 1993, Vol.100 (2), p.186S-190S [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0022-202X ;EISSN: 1523-1747 ;CODEN: JIDEAE

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15
Treatment of port-wine stains (capillary malformation) with the flashlamp-pumped pulsed dye laser
Material Type:
Article
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Treatment of port-wine stains (capillary malformation) with the flashlamp-pumped pulsed dye laser

The Journal of pediatrics, 1993, Vol.122 (1), p.71-77 [Peer Reviewed Journal]

1993 Mosby-Year Book, Inc. All rights reserved ;1993 INIST-CNRS ;ISSN: 0022-3476 ;EISSN: 1097-6833 ;DOI: 10.1016/S0022-3476(05)83489-4 ;PMID: 8419617 ;CODEN: JOPDAB

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16
The blue rubber bleb syndrome
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Article
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The blue rubber bleb syndrome

Journal of the Pakistan Medical Association, 1993, Vol.43 (1), p.20-21

1993 INIST-CNRS ;ISSN: 0030-9982 ;PMID: 8474216 ;CODEN: JJPAD4

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17
Focal dermal hypoplasia (Goltz syndrome): An adult case with multisystemic involvement
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Article
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Focal dermal hypoplasia (Goltz syndrome): An adult case with multisystemic involvement

Journal of the American Academy of Dermatology, 1993, Vol.28 (1), p.86-89 [Peer Reviewed Journal]

1993 American Academy of Dermatology, Inc. ;1993 INIST-CNRS ;ISSN: 0190-9622 ;EISSN: 1097-6787 ;DOI: 10.1016/0190-9622(93)70015-L ;PMID: 8425976 ;CODEN: JAADDB

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18
Gastrointestinal involvement in a women with dyskeratosis congenita
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Article
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Gastrointestinal involvement in a women with dyskeratosis congenita

Digestive diseases and sciences, 1993, Vol.38 (1), p.181-184 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0163-2116 ;EISSN: 1573-2568 ;CODEN: DDSCDJ

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19
A xerodermal pigmentosum complementation group A related gene : confirmation using monoclonal antibodies against the cyclobutane dimer and (6-4) photoproduct
Material Type:
Article
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A xerodermal pigmentosum complementation group A related gene : confirmation using monoclonal antibodies against the cyclobutane dimer and (6-4) photoproduct

Mutation research. DNA repair, 1993, Vol.293 (2), p.143-150

1993 INIST-CNRS ;ISSN: 0921-8777 ;EISSN: 1386-1476

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20
Identification of Six New Gaucher Disease Mutations
Material Type:
Article
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Identification of Six New Gaucher Disease Mutations

Genomics (San Diego, Calif.), 1993, Vol.15 (1), p.203-205 [Peer Reviewed Journal]

1993 Academic Press ;1993 INIST-CNRS ;ISSN: 0888-7543 ;EISSN: 1089-8646 ;DOI: 10.1006/geno.1993.1035 ;PMID: 8432537

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