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Journal Abstract Search

115 related items for PubMed ID: 1723388

  • 21. [The oto-palato-digital syndrome (Taybi) (author's transl)].
    Szabó L, Perjés K, Mangliár K.
    Z Orthop Ihre Grenzgeb; 1977 Feb; 115(1):75-82. PubMed ID: 842092
    [Abstract] [Full Text] [Related]

  • 22. Development and behaviour in Marshall-Smith syndrome: an exploratory study of cognition, phenotype and autism.
    van Balkom ID, Shaw A, Vuijk PJ, Franssens M, Hoek HW, Hennekam RC.
    J Intellect Disabil Res; 2011 Oct; 55(10):973-87. PubMed ID: 21790824
    [Abstract] [Full Text] [Related]

  • 23. [Unusual syndrome with acceleration of skeletal maturation (Marshall's syndrome). 1st case in the Italian literature].
    De Toni E, Duillo MT, De Toni T, Cortese M, Bergamo F.
    Minerva Pediatr; 1976 Jul 28; 28(24):1499-509. PubMed ID: 1012192
    [No Abstract] [Full Text] [Related]

  • 24. Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet.
    Waldrop MA, Boue DR, Sites E, Flanigan KM, Shell R.
    Pediatr Neurol; 2017 Sep 28; 74():11-14. PubMed ID: 28676249
    [No Abstract] [Full Text] [Related]

  • 25. Functional outcome at school age of preterm infants with periventricular hemorrhagic infarction.
    Roze E, Van Braeckel KN, van der Veere CN, Maathuis CG, Martijn A, Bos AF.
    Pediatrics; 2009 Jun 28; 123(6):1493-500. PubMed ID: 19482759
    [Abstract] [Full Text] [Related]

  • 26. Early developmental trajectories of males with fragile X syndrome.
    Bailey DB, Hatton DD, Skinner M.
    Am J Ment Retard; 1998 Jul 28; 103(1):29-39. PubMed ID: 9678228
    [Abstract] [Full Text] [Related]

  • 27. Short case presentation. Pierre-Robin sequence.
    Dinwiddie R.
    Paediatr Respir Rev; 2004 Mar 28; 5(1):90, 92. PubMed ID: 15230265
    [No Abstract] [Full Text] [Related]

  • 28. General movements in very preterm children and neurodevelopment at 2 and 4 years.
    Spittle AJ, Spencer-Smith MM, Cheong JL, Eeles AL, Lee KJ, Anderson PJ, Doyle LW.
    Pediatrics; 2013 Aug 28; 132(2):e452-8. PubMed ID: 23878041
    [Abstract] [Full Text] [Related]

  • 29. Evaluation for language and speech development in Kabuki make-up syndrome: a case report.
    Bayar Muluk N, Yalçinkaya F, Budak B, Gündüz S, Ayas K.
    Int J Pediatr Otorhinolaryngol; 2009 Dec 28; 73(12):1837-40. PubMed ID: 19853311
    [Abstract] [Full Text] [Related]

  • 30. [Early psychomotor development--normal and abnormal. References for the detection and evaluation of development disorders].
    Largo RH.
    Schweiz Rundsch Med Prax; 1985 Feb 26; 74(9):203-6. PubMed ID: 2580341
    [No Abstract] [Full Text] [Related]

  • 31. Prediction of preschool sensory and motor performance by 18-month neurologic scores among children born prematurely.
    Lane SJ, Attanasio CS, Huselid RF.
    Am J Occup Ther; 1994 May 26; 48(5):391-6. PubMed ID: 8042681
    [Abstract] [Full Text] [Related]

  • 32. Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of the literature.
    Klinge L, Schaper J, Wieczorek D, Voit T.
    Neuropediatrics; 2002 Dec 26; 33(6):309-13. PubMed ID: 12571786
    [Abstract] [Full Text] [Related]

  • 33. [Principal psychopathologic disorders of childhood].
    Braconnier A.
    Soins Psychiatr; 1982 Mar 26; (17):34-8. PubMed ID: 6177053
    [No Abstract] [Full Text] [Related]

  • 34. Identical twins with Weissenbacher-Zweymüller syndrome and neural tube defect.
    Ramer JC, Eggli K, Rogan PK, Ladda RL.
    Am J Med Genet; 1993 Mar 01; 45(5):614-8. PubMed ID: 8456835
    [Abstract] [Full Text] [Related]

  • 35. [Bright ocular background with profound cutis laxa and large fontanelles].
    Marjanovic I, Seitz B, Käsmann-Kellner B.
    Ophthalmologe; 2015 Jan 01; 112(1):64-6. PubMed ID: 25573084
    [No Abstract] [Full Text] [Related]

  • 36. Development of early motor skills and language in children at risk for familial dyslexia.
    Viholainen H, Ahonen T, Cantell M, Lyytinen P, Lyytinen H.
    Dev Med Child Neurol; 2002 Nov 01; 44(11):761-9. PubMed ID: 12418617
    [Abstract] [Full Text] [Related]

  • 37. Kniest disease.
    Spranger JW, Maroteaux P.
    Birth Defects Orig Artic Ser; 1974 Nov 01; 10(12):50-6. PubMed ID: 4461083
    [No Abstract] [Full Text] [Related]

  • 38. A new syndrome: congenital thrombocytopenia, Robin sequence, agenesis of the corpus callosum, distinctive facies and developmental delay.
    Braddock SR, Carey JC.
    Clin Dysmorphol; 1994 Jan 01; 3(1):75-81. PubMed ID: 7515754
    [Abstract] [Full Text] [Related]

  • 39. Motor incoordination in children born preterm: coordinated efforts needed.
    Majnemer A.
    Dev Med Child Neurol; 2007 May 01; 49(5):324. PubMed ID: 17489803
    [No Abstract] [Full Text] [Related]

  • 40. Diagnostic criteria for Rett syndrome. The Rett Syndrome Diagnostic Criteria Work Group.
    Ann Neurol; 1988 Apr 01; 23(4):425-8. PubMed ID: 2454607
    [Abstract] [Full Text] [Related]

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