Biomedical subjects

R J GORLIN

Publications and source records attributed to R J GORLIN.

At least 19 recordsLinked to original sources

PubMed1965

MULTIPLE BASAL-CELL NEVI SYNDROME. AN ANALYSIS OF A SYNDROME CONSISTING OF MULTIPLE NEVOID BASAL-CELL CARCINOMA, JAW CYSTS, SKELETAL ANOMALIES, MEDULLOBLASTOMA, AND HYPORESPONSIVENESS TO PARATHORMONE.

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Adolescent↗

PubMed1965

A PSYCHOLOGICAL COMPONENT IN THE ETIOLOGY OF GEOGRAPHIC TONGUE.

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Glossitis↗

PubMed1965

ABNORMAL MORPHOLOGY OF THE SOFT PALATE. II. THE GENETICS OF CLEFT UVULA.

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Cleft Palate↗

PubMed1965

THE LIBRARY IN DENTAL RESEARCH.

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Dental Research↗

PubMed1965

TORUS MANDIBULARIS: A GENETICS STUDY.

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Adolescent↗

PubMed1964

POSSIBLE ANALOGOUS CUTANEOUS AND ODONTOGENIC TUMORS.

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Calcification, Physiologic↗

PubMed1964

THE CALCIFYING ODONTOGENIC CYST. A NEW ENTITY AND POSSIBLE ANALOGUE OF THE CUTANEOUS CALCIFYING EPITHELIOMA OF MALHERBE.

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Calcification, Physiologic↗

PubMed1964

AN ANALYSIS OF ORAL CYTODIAGNOSIS.

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Cytodiagnosis↗

PubMed1964

CHROMOSOMAL ABNORMALITIES AND ORAL ANOMALIES.

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Chromosome Aberrations↗

PubMed1964

THE ROLE OF EXFOLIATIVE CYTOLOGY IN ORAL CANCER DETECTION.

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Cytodiagnosis↗

PubMed1964

THE SYNDROME OF PALMAR-PLANTAR HYPERKERATOSIS AND PREMATURE PERIODONTAL DESTRUCTION OF THE TEETH. A CLINICAL AND GENETIC ANALYSIS OF THE PAPILLON-LEF'EVRE SYNDROME.

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Acrodynia↗

PubMed1964

ORAL TUMORS OF INFANCY.

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Humans↗

PubMed1964

OCCURRENCE OF HETEROTOPIC GASTRIC MUCOSA IN THE TONGUE.

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Child↗

PubMed1964

ABNORMAL MORPHOLOGY OF THE SOFT PALATE. I. THE PREVALENCE OF CLEFT UVULA.

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Biometry↗

PubMed1964

GROSS CHROMOSOMAL ABNORMALITY. CLINICAL AND LABORATORY AIDS IN THE DIAGNOSIS.

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Chromosome Aberrations↗

PubMed1963

ODONTOGENIC TUMORS IN MAN AND ANIMALS: PATHOLOGIC CLASSIFICATION AND CLINICAL BEHAVIOR. A REVIEW.

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Animals, Domestic↗

PubMed1963

Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome.

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Basal Cell Carcinoma↗

PubMed1963

The oral manifestations of cyclopia. Review of the literature and report of two cases.

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Holoprosencephaly↗