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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

144 related items for PubMed ID: 9072822

  • 61.
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  • 62. A gene for ulnar-mammary syndrome maps to 12q23-q24.1.
    Bamshad M, Krakowiak PA, Watkins WS, Root S, Carey JC, Jorde LB.
    Hum Mol Genet; 1995 Oct; 4(10):1973-7. PubMed ID: 8595424
    [Abstract] [Full Text] [Related]

  • 63. Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.
    Crackower MA, Scherer SW, Rommens JM, Hui CC, Poorkaj P, Soder S, Cobben JM, Hudgins L, Evans JP, Tsui LC.
    Hum Mol Genet; 1996 May; 5(5):571-9. PubMed ID: 8733122
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  • 64. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
    Leichtman LG, Zackowski JL, Storto PD, Newlin A.
    Am J Med Genet; 1996 Jun 14; 63(3):434-7. PubMed ID: 8737648
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  • 65. Mirror image duplication of the hands and feet: report of a sporadic case with multiple congenital anomalies.
    Hersh JH, Dela Cruz TV, Pietrantoni M, von Drasek-Ascher G, Turnquest MA, Yacoub OA, Joyce MR.
    Am J Med Genet; 1995 Nov 20; 59(3):341-5. PubMed ID: 8599358
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  • 66. The hand-foot-genital (hand-foot-uterus) syndrome: family report and update.
    Halal F.
    Am J Med Genet; 1988 Jul 20; 30(3):793-803. PubMed ID: 3189398
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  • 67.
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  • 68. Tibial hemimelia: report on 37 new cases, clinical and genetic considerations.
    Richieri-Costa A, Ferrareto I, Masiero D, da Silva CR.
    Am J Med Genet; 1987 Aug 20; 27(4):867-84. PubMed ID: 3425598
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  • 69. Split hand/split foot deformity and LADD syndrome in a family: overlap between the EEC and LADD syndromes.
    Lacombe D, Serville F, Marchand D, Battin J.
    J Med Genet; 1993 Aug 20; 30(8):700-3. PubMed ID: 8411061
    [Abstract] [Full Text] [Related]

  • 70. Is brachydactyly type Ballard a variant of brachydactyly type E?
    Jensen K, Hoo JJ.
    Am J Med Genet A; 2004 Aug 15; 129A(1):95-7. PubMed ID: 15266625
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  • 71.
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  • 72.
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  • 73.
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  • 74.
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  • 75. Skeletal malformations and polycystic kidney disease.
    Winter RM.
    J Med Genet; 1993 Nov 15; 30(11):973. PubMed ID: 8301661
    [No Abstract] [Full Text] [Related]

  • 76. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C, Carvajal MV, Moscatello D, Towner J, Lacassie Y.
    Am J Med Genet; 1995 Mar 13; 56(1):1-5. PubMed ID: 7747769
    [Abstract] [Full Text] [Related]

  • 77. Smith-Lemli-Opitz syndrome: the changing phenotype with age.
    de Die-Smulders C, Fryns JP.
    Genet Couns; 1992 Mar 13; 3(2):77-82. PubMed ID: 1642814
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  • 78.
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  • 79.
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  • 80. [Multiple synostosis syndrome].
    Alessandri C, Bellussi A.
    Minerva Pediatr; 1989 Dec 13; 41(12):619-21. PubMed ID: 2634814
    [Abstract] [Full Text] [Related]

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