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au.\*:("RIMOIN DL")

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PATHOGENETIC MECHANISMS OF LIMB MALFORMATION IN THE SKELETAL DYSPLASIAS.RIMOIN DL.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 1; PP. 339-353; BIBL. 16 REF.; (MORPHOG. MALFORM. LIMB. INT. CONF. MORPHOG. MALFORM. 2; TITISEE; 1975)Conference Paper

INTERNATIONAL NOMENCLATURE OF CONSTITUTIONAL DISEASES OF BONE: REVISION-MAY 1977RIMOIN DL.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6B; PP. 39-45Article

INTERNATIONAL NOMENCLATURE OF CONSTITUTIONAL DISEASES OF BONE: REVISION-MAY 1977RIMOIN DL.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 3; NO 1; PP. 21-26Article

VARIABLE EXPRESSIVITY IN THE SKELETAL DYSPLASIASRIMOIN DL.1979; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1979; VOL. 15; NO 5B; PP. 91-112; BIBL. 14 REF.Article

THE CHONDRODYSTROPHIESRIMOIN DL.1975; ADV. HUM. GENET.; U.S.A.; DA. 1975; VOL. 5; PP. 1-118; BIBL. 15 P. 1/2Article

HETEROGENEITY IN DIABETES MELLITUS-UPDATE, 1978. EVIDENCE FOR FURTHER GENETIC HETEROGENEITY WITHIN JUVENILE-ONSET INSULIN-DEPENDENT DIABETES MELLITUS.ROTTER JI; RIMOIN DL.1978; DIABETES; USA; DA. 1978; VOL. 27; NO 5; PP. 599-605; BIBL. 59 REF.Article

HISTOCHEMICAL CHARACTERIZATION OF THE ENDOCHONDRAL GROWTH PLATE: A NEW APPROACH TO THE STUDY OF THE CHONDRODYSTROPHIESHORTON WA; RIMOIN DL.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6B; PP. 81-93; BIBL. 10 REF.Article

KNIEST DYSPLASIA. A HISTOCHEMICAL STUDY OF THE GROWTH PLATEHORTON WA; RIMOIN DL.1979; PEDIATR. RES.; USA; DA. 1979; VOL. 13; NO 11; PP. 1266-1270; BIBL. 16 REF.Article

ADDITIONAL COMMENTS ON THE ULCER-MULTIPLE LENTIGINES SYNDROMEROTTER JI; RIMOIN DL.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 2; PP. 251-252; BIBL. 13 REF.Article

A NEW AUTOSOMAL DOMINANT SYNDROME OF HYPOHIDROTIC ECTODERMAL DYSPLASIA AND UNUSUAL FACIESBOCIAN M; RIMOIN DL.1979; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1979; VOL. 15; NO 5B; PP. 239-251; BIBL. 25 REF.Article

THE PYGMY (PG) MUTANT OF THE MOUSE. A MODEL OF THE HUMAN PYGMY = LE MUTANT PYGMEE (PG) DE LA SOURIS, MODELE DU PYGMEE HUMAINRIMOIN DL; RICHMOND L.1972; J. CLIN. ENDOCRINOL. METABOL.; U.S.A.; DA. 1972; VOL. 35; NO 3; PP. 467-468; BIBL. 6REF.Article

THE GENETIC SYNDROMOLOGY OF PEPTIC ULCERROTTER JI; RIMOIN DL.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 10; NO 4; PP. 315-321; BIBL. 2 P.Article

MEDICAL PROGRESS. SHORT STATURE. II.RIMOIN DL; HORTON WA.1978; J. PEDIATR.; U.S.A.; DA. 1978; VOL. 92; NO 5; PP. 697-704; BIBL. 36 REF.Article

SHORT NATURE. I.RIMOIN DL; HORTON WA.1978; J. PEDIATR.; U.S.A.; DA. 1978; VOL. 92; NO 4; PP. 523-528; BIBL. 16 REF.Article

MORPHOLOGIC STUDIES IN THE SKELETAL DYSPLASIAS: A REVIEWSILLENCE DO; HORTON WA; RIMOIN DL et al.1979; AMER. J. PATHOL.; USA; DA. 1979; VOL. 96; NO 3; PP. 813-870; BIBL. 295 REF.Article

CLINICAL VARIABILITY IN OSTEOGENESIS IMPERFECTA-VARIABLE EXPRESSIVITY OR GENETIC HETEROGENEITYSILLENCE DO; RIMOIN DL; DANKS DM et al.1979; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1979; VOL. 15; NO 5B; PP. 113-129; BIBL. 66 REF.Article

NEONATAL DWARFISMSILLENCE DO; RIMOIN DL; LACHMAN R et al.1978; PEDIATR. CLIN. N. AMER.; USA; DA. 1978; VOL. 25; NO 3; PP. 453-483; BIBL. 46 REF.Article

PSYCHIATRIC ASPECTS OF DIVARFISM. = ASPECTS PSYCHIATRIQUES DU NANISMEBRUST JS; FORD CV; RIMOIN DL et al.1976; AMER. J. PSYCHIATRY; U.S.A.; DA. 1976; VOL. 133; NO 2; PP. 160-164; BIBL. 21 REF.Article

A NEW VARIANT OF DANLOS SYNDROME: AN AUTOSOMAL DOMINANT DISORDER OF FRAGILE SKIN, ABNORMAL SCARRING, AND GENERALIZED PERIODONTITIS.STEWART RE; HOLLISTER DW; RIMOIN DL et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 85-93; BIBL. 7 REF.Article

MACROCEPHALY WITH MULTIPLE LIPOMAS AND HEMANGIOMAS.ZONANA J; RIMOIN DL; DAVIS DC et al.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 89; NO 4; PP. 600-603; BIBL. 8 REF.Article

MESOMELIC SKELETAL DYSPLASIASKAITILA II; LEISTI JT; RIMOIN DL et al.1976; CLIN. ORTHOP. RELAT. RES.; U.S.A.; DA. 1976; VOL. 114; NO 1; PP. 94-106; BIBL. 1 P. 1/2Article

HUMAN X-AUTOSOME TRANSLOCATIONS: DIFFERENTIAL INACTIVATION OF THE X CHROMOSOME IN A KINDRED WITH AN X-9 TRANSLOCATION = TRANSLOCATIONS HUMAINES X-AUTOSOME: INACTIVATION DIFFERENTIELLE DU CHROMOSOME X DANS UNE FAMILLE AYANT UNE TRANSLOCATION X-9LEISTI JT; KABACK MM; RIMOIN DL et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 27; NO 4; PP. 441-453; BIBL. 1 P. 1/2Article

HIP ARTHROGRAPHY IN THE EPIPHYSEAL DYSPLASIAS = ARTHROGRAPHIE DE HANCHE DANS LES DYSPLASIES EPIPHYSAIRESLACHMAN RS; RIMOIN DL; HOLLISTER DW et al.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 12; PP. 186-195; BIBL. 1REF.Article

CHONDRO-OSSEOUS PATHOLOGY IN THE CHONDRODYSTROPHIESRIMOIN DL; SILBERBERG R; HOLLISTER DW et al.1976; CLIN. ORTHOP. RELAT. RES.; U.S.A.; DA. 1976; VOL. 114; NO 1; PP. 137-152; BIBL. 1 P. 1/2Article

IDENTIFICATION BY FLUORESCENT MICROSCOPY OF THE ABNORMAL CHROMOSOMES ASSOCIATED WITH THE G-DELETION SYNDROMES = IDENTIFICATION PAR MICROSCOPIE DE FLUORESCENCE DES CHROMOSOMES ANORMAUX ASSOCIES AUX SYNDROMES DE DELETION GWARREN RJ; RIMOIN DL; SUMMITT RL et al.1973; AMER. J. HUM. GENET.; U.S.A.; DA. 1973; VOL. 25; NO 1; PP. 77-81; BIBL. 14REF.Serial Issue

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