These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

77 related articles for article (PubMed ID: 1218236)

  • 1. Familial multiforme ventricular extrasystoles with short stature, hyperpigmentation and microcephaly-a new syndrome.
    Char F; Douglas JE; Dungan WT
    Birth Defects Orig Artic Ser; 1975; 11(5):63-9. PubMed ID: 1218236
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A syndrome of microcephaly, eye anomalies, short stature, and mental deficiency.
    Bouwes Bavinck JN; Weaver DD; Ellis FD; Ward RE
    Am J Med Genet; 1987 Apr; 26(4):825-31. PubMed ID: 3109242
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation: a possible "new" form of ectodermal dysplasia.
    Winter RM; MacDermot KD; Hill FJ
    Am J Med Genet; 1988 Jan; 29(1):209-16. PubMed ID: 3344769
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new X-linked mental retardation (XLMR) syndrome with late-onset primary testicular failure, short stature and microcephaly maps to Xq25-q26.
    Cilliers DD; Parveen R; Clayton P; Cairns SA; Clarke S; Shalet SM; Black GC; Newman WG; Clayton-Smith J
    Eur J Med Genet; 2007; 50(3):216-23. PubMed ID: 17369115
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin in sequence in three generations: a new inherited MCA syndrome?
    Stoll C; Kieny JR; Dott B; Alembik Y; Finck S
    Am J Med Genet; 1992 Feb; 42(4):480-6. PubMed ID: 1376967
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Familial syndrome combining short stature, microcephaly, mental deficiency, seizures, hearing loss, and skin lesions. A new syndrome].
    Boudhina T; Yedes A; Khiari S; Ghram N; Ben Becher S; Makni S; Ben Jemaa M; Hamza M
    Ann Pediatr (Paris); 1990 Jun; 37(6):399-403. PubMed ID: 2400194
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new case of Martsolf syndrome.
    Bora E; Cankaya T; Alpman A; Karaca E; Cogulu O; Tekgul H; Ozkinay F
    Genet Couns; 2007; 18(1):71-5. PubMed ID: 17515302
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.
    Martínez-Frías ML; Martín M; Pardo M; Fernandez de las Heras F; Frías JL
    Am J Med Genet; 1995 Jan; 55(2):213-6. PubMed ID: 7717420
    [TBL] [Abstract][Full Text] [Related]  

  • 9. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L; Corsello G; Giuffrè M; Piccione M; Albanese A
    Am J Med Genet; 1994 Jul; 51(3):266-9. PubMed ID: 8074157
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bigeminal rhythm due to reentrant ventricular extrasystoles coupled to ventricular and A-V junctional escapes: comparison with ventricular parasystole associated with ventricular extrasystoles of bundle branch reentry.
    Izumi K
    Mater Med Pol; 1989; 21(3):213-22. PubMed ID: 2485075
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Ring chromosome 14. II. A case report of r(14) mosaicism. The r(14) phenotype].
    Rethoré MO; Caille B; Huet de Barochez Y; de Blois MC; Ravel A; Lejeune J
    Ann Genet; 1984; 27(2):91-5. PubMed ID: 6331796
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tall stature, microcephaly, hypotonia, advanced bone age, and unusual infra-auricular creases.
    Stratton RF
    Am J Med Genet; 1998 Jan; 75(3):261-2. PubMed ID: 9475593
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
    Tsukahara M; Sugio Y
    J Hum Genet; 1998; 43(4):224-7. PubMed ID: 9852671
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?
    Mégarbané A; Choueiri R; Bleik J; Mezzina M; Caillaud C
    J Med Genet; 1999 Aug; 36(8):637-40. PubMed ID: 10465117
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Drayer's syndrome of mental retardation, microcephaly, short stature and absent phalanges is caused by a recurrent deletion of chromosome 15(q26.2-->qter).
    Rump P; Dijkhuizen T; Sikkema-Raddatz B; Lemmink HH; Vos YJ; Verheij JB; van Ravenswaaij CM
    Clin Genet; 2008 Nov; 74(5):455-62. PubMed ID: 18651844
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face.
    Winter RM
    Am J Med Genet; 1993 Nov; 47(6):917-20. PubMed ID: 7506485
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microcephaly, hypergonadotropic hypogonadism, short stature, and minor anomalies: a new syndrome.
    Mikati MA; Najjar SS; Sahli IF; Melhem RE; Mansour S; Der Kaloustian VM
    Am J Med Genet; 1985 Nov; 22(3):599-608. PubMed ID: 2998187
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F
    Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome).
    Abu-Libdeh B; Fujimoto A; Ehinger M
    Am J Med Genet; 1993 Feb; 45(3):358-60. PubMed ID: 8434624
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new familial metabolic disorder with progressive osseous changes, microcephaly, coarse facies, flat nasal bridge and severe mental retardation.
    Hall BD; Riggs FD
    Birth Defects Orig Artic Ser; 1975; 11(5):79-90. PubMed ID: 1218240
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.