Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("BRACHYPHALANGY")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 26

  • Page / 2
Export

Selection :

  • and

Brachymetacarpia and brachyphalangiaMIURA, T; TORII, S; NAKAMYURA, R et al.The Journal of hand surgery (St. Louis, Mo.). 1986, Vol 11, Num 6, pp 829-836, issn 0363-5023Article

Cryptomicrotia and short, stubby fingers with excess fingertip arch patterns in a mother and sonTONOKI, H; OHURA, T; NIIKAWA, N et al.American journal of medical genetics. 1988, Vol 29, Num 4, pp 857-862, issn 0148-7299Article

Brachytéléphalangie révélée à l'occasion de dystrophies unguéales induites par cryothérapie = Brachytelephalangy revealed by onychodystrophy secondary to liquid nitrogen therapyBARAN, R.Annales de dermatologie et de vénéréologie. 1985, Vol 112, Num 4, pp 365-367, issn 0151-9638Article

BRACHYMESOPHALANGY AND LOOSE BODIES IN THE METACARPOPHALANGEAL JOINTSBOE S; LUCHT U.1979; ACTA ORTHOP. SCAND.; DNK; DA. 1979; VOL. 50; NO 6 PART. 2; PP. 755-758; BIBL. 7 REF.Article

Additional Features in a New Case of a Girl Presenting Brachyphalangy, Polydactyly and Tibial Aplasia/HypoplasiaBERNARDI, Pricila; GRAZIADIO, Carla; ROSA, Rafael F. M et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 7, pp 1532-1538, issn 1552-4825, 7 p.Article

DISTAL SYMPHALANGISM: SYMBRACHYDACTYLISM ARISING IN A FAMILY WITH DISTAL SYMPHALANGISMHALPERN AA; WHEELER RD; SCHURMAN DJ et al.1979; CLIN. ORTHOP. RELAT. RES.; USA; DA. 1979; NO 141; PP. 251-255; BIBL. 15 REF.Article

RADIOGRAPHIE DES PHALANGES ET DU METACARPE DANS LE SYMPHALANGIQUE ET LA BRACHYMESOPHALANGIE 5. DONNEES CLINIQUES ET GENETIQUESCUNHA AJB; BRUNONI D; ESPER R et al.1978; CI. E CULT.; BRA; DA. 1978; VOL. 30; NO 10; PP. 1237-1241; ABS. ENG; BIBL. 12 REF.Article

Keutel syndrome: clinical report and literature reviewCORMODE, E. J; DAWSON, M; LOWRY, R. B et al.American journal of medical genetics. 1986, Vol 24, Num 2, pp 289-294, issn 0148-7299Article

A new type of a lethal osteochodrodysplasia with angel-shaped brachyphalangyCADUFF, R; GIEDION, A; BRINER, J et al.Virchows Archiv. 1994, Vol 424, Num 1, pp 113-119, issn 0945-6317Article

Calcification of cartilages, barchytelephalangy and peripheral pulmonary stenosis: confirmation of the Keutel syndromeFRYNS, J. P; VAN FLETEREN, A; MATTELAER, P et al.European journal of pediatrics. 1984, Vol 142, Num 3, pp 201-203, issn 0340-6199Article

Brachyphalangy, polydactyly and tibial aplasia/hypoplasia syndrome (OMIM 609945): case report and review of the literatureSHAFEGHATI, Yousef; KAHRIZI, Kimia; NAJMABADI, Hossein et al.European journal of pediatrics. 2010, Vol 169, Num 12, pp 1535-1539, issn 0340-6199, 5 p.Article

ABNORMAL METACARPAL HEADS IN BRACHYMESOPHALANGY: REPORT OF A CASE AND REVIEW OF THE LITERATURERENTON P; HALLETT JP.1981; J. HAND SURG.; ISSN 0363-5023; USA; DA. 1981; VOL. 6; NO 6; PP. 545-549; BIBL. 5 REF.Article

Mosaic monosomy of a neocentric ring chromosome maps brachyphalangy and growth hormone deficiency to 13q31.1-13q32.3AMOR, David J; VOULLAIRE, Lucille; BENTLEY, Karen et al.American journal of medical genetics. 2005, Vol 133A, Num 2, pp 151-157, issn 0148-7299, 7 p.Article

Syndactyly/brachyphalangy and nail dysplasias as marker lesions for sclerosteosisITIN, Peter H; KESERÜ, Borbala; HAUSER, Vital et al.Dermatology (Basel). 2001, Vol 202, Num 3, pp 259-260, issn 1018-8665Article

An unusual carpal coalition associated with fifth ray anomalies in the handGOMEZ ROBLEDO, J.Journal of hand surgery. British and european volume. 1998, Vol 23, Num 4, pp 537-538Article

PRE AND POST AXIAL POLYSYNDACTYLY MICROCEPHAL AND PTOSISENGELHARD D; YATZIV S.1979; EUROP. J. PEDIATR.; DEU; DA. 1979; VOL. 130; NO 1; PP. 47-51; BIBL. 6 REF.Article

Characteristic craniofacial appearance and brachytelephalangy in a mother and son with Kallman syndrome in the sonHUNTER, A. G. W; FELDMAN, W; MILLER, J et al.American journal of medical genetics. 1986, Vol 24, Num 3, pp 527-532, issn 0148-7299Article

THE INTERFRONTAL BONE AND MUTANT GENES IN THE MOUSE. = L'OS WORMIEN FRONTO-NASAL ET LES GENES MUTANTS CHEZ LA SOURISJOHNSON DR.1976; J. ANAT.; G.B.; DA. 1976; VOL. 121; NO 3; PP. 507-513; BIBL. 23 REF.Article

Hand involvement in 13q Deletion syndromeGRINDEL, S. I; SANDLIN, C; WOOD, V. E et al.Journal of pediatric orthopedics. 1999, Vol 19, Num 5, pp 620-623, issn 0271-6798Article

Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive formMAROTEAUX, P.Human genetics. 1989, Vol 82, Num 2, pp 167-170, issn 0340-6717Article

An apparently new autosomal recessive syndrome with facial dysmorphism, macrocephaly, myopia and Dandy-Walker malformationBUTTIENS, M; FRYNS, J. P; VAN DEN BERGHE, H et al.Clinical genetics. 1989, Vol 36, Num 6, pp 451-455, issn 0009-9163Article

The MMT syndrome: a newly recognized benign microcephalyBUYSE, M. L.Dysmorphology and clinical genetics. 1990, Vol 4, Num 3, pp 81-82, 2 p.Article

Foetopathie coumarinique = Warfarin embryopathyBONY, C; ZYKA, F; TIRAN-RAJAOFERA, I et al.Archives de pédiatrie (Paris). 2002, Vol 9, Num 7, pp 705-708, issn 0929-693XArticle

Cryptophthalmos, dental and oral abnormalities, and brachymesophalangy of second toes : New syndrome or Fraser syndrome?KANTAPUTRA, Piranit N; EIUMTRAKUL, Pakanart; MATIN, Tada et al.American journal of medical genetics. 2001, Vol 98, Num 3, pp 263-268, issn 0148-7299Article

Microcephaly, mesobrachyphalangy, and tracheoesophageal fistula: MMT syndromeKÖNIG, R; SELZER, G; STOLP, A et al.Dysmorphology and clinical genetics. 1990, Vol 4, Num 3, pp 83-86, 4 p.Article

  • Page / 2