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Journal Abstract Search
152 related items for PubMed ID: 6661523
1. Heterogeneity in the trichorhinophalangeal syndromes. Jorgenson RJ, Salinas CF, Sujansky E, Beierle LE. Birth Defects Orig Artic Ser; 1983; 19(1):167-79. PubMed ID: 6661523 [No Abstract] [Full Text] [Related]
2. [Trichorhinophalangeal syndrome--clinical presentation and genetics]. Brodwall KM, Júlíusson PB, Bjerknes R, Hovland R, Fiskerstrand T. Tidsskr Nor Laegeforen; 2011 Aug 09; 131(15):1420-3. PubMed ID: 21844942 [Abstract] [Full Text] [Related]
3. Facial and oral findings in trichorhinophalangeal syndrome type 1 (characteristics of TRPS 1). Bennett CG, Hill CJ, Frias JL. Pediatr Dent; 1981 Dec 09; 3(4):348-52. PubMed ID: 6952172 [No Abstract] [Full Text] [Related]
4. A familial case of tricho-rhino-phalangeal syndrome type III with a novel missense mutation in exon 6 of the TRPS1 gene. Sendi-Naderi A, Lüdecke HJ, Unger S, Kern JS, Wolff G, Bruckner-Tuderman L, Nashan D. J Eur Acad Dermatol Venereol; 2010 May 09; 24(5):612-4. PubMed ID: 19758263 [No Abstract] [Full Text] [Related]
6. [Trichorhinophalangeal syndrome : analysis of craniofacial architecture in six cases (author's transl)]. Scheffer P, Verdier M, Finidori G. Rev Stomatol Chir Maxillofac; 1981 May 09; 82(4):230-3. PubMed ID: 6944759 [Abstract] [Full Text] [Related]
7. [New hereditary syndrome with mental retardation]. Marincheva GS, Kupriianova TA, Batienko GS. Zh Nevropatol Psikhiatr Im S S Korsakova; 1988 May 09; 88(3):69-74. PubMed ID: 3381618 [Abstract] [Full Text] [Related]
8. Variable expressivity in the trichorhinophalangeal syndrome type I. Frias JL, Felman AH, Garnica AD, Wallace SE. Birth Defects Orig Artic Ser; 1979 May 09; 15(5B):361-72. PubMed ID: 526590 [No Abstract] [Full Text] [Related]
13. Trichorhinophalangeal syndrome type I and systemic lupus erythematosus with complement C4A homozygous null alleles in the same family. Dahlqvist SR, Lundström B, Holmgren G. Ann Rheum Dis; 1989 Sep 09; 48(9):760-4. PubMed ID: 2802798 [Abstract] [Full Text] [Related]
15. Naxos disease and Carvajal syndrome: cardiocutaneous disorders that highlight the pathogenesis and broaden the spectrum of arrhythmogenic right ventricular cardiomyopathy. Protonotarios N, Tsatsopoulou A. Cardiovasc Pathol; 2004 Sep 09; 13(4):185-94. PubMed ID: 15210133 [Abstract] [Full Text] [Related]
18. Trichorhinophalangeal syndrome as a diagnostic and therapeutic challenge for paediatric endocrinologists. Foryś-Dworniczak E, Zajdel-Cwynar O, Kalina-Faska B, Małecka-Tendera E, Matusik P. Pediatr Endocrinol Diabetes Metab; 2019 Sep 09; 25(1):41-47. PubMed ID: 31343132 [Abstract] [Full Text] [Related]
19. [Genetic counseling in a case of neuro-ectodermosis: Vera Price trichothiodystrophy. Brittle hair with reduced sulfur content]. Poissonnier M, Blanc A, Bat P. J Genet Hum; 1988 Aug 09; 36(4):361-5. PubMed ID: 3221211 [No Abstract] [Full Text] [Related]
20. [A case of dystonia musculorum deformans in a patient with type I trichorhinophalangeal dysplasia]. Malyshev IuI, Mal'mberg SA, Solonichenko VG, Chuchin MIu. Pediatriia; 1992 Aug 09; (1):102-6. PubMed ID: 1614793 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]