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 *

75 related articles for article (PubMed ID: 8825936)

  • 21. Holoprosencephaly in a fetus with a 46,XX,der(7), t(7;8)(q36.1;p12) mat karyotype.
    Kleczkowska A; Fryns JP; Moerman P; Vandenberghe K; Van den Berghe H
    Ann Genet; 1990; 33(2):111-2. PubMed ID: 2241084
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Riyadh chromosome breakage syndrome: mental retardation with depigmentation of the skin and hair.
    Ozand PT; Waghray M; Cook JD; Sheth K; Gascon GG
    J Child Neurol; 1992 Apr; 7 Suppl():S79-82. PubMed ID: 1588019
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Trisomy 18 with unilateral atypical ectrodactyly.
    Rogers RC
    Am J Med Genet; 1994 Jan; 49(1):125-7. PubMed ID: 8172239
    [No Abstract]   [Full Text] [Related]  

  • 24. Genetic factors in the determination of fetal size.
    Jones OW
    J Reprod Med; 1978 Nov; 21(5):305-13. PubMed ID: 153400
    [No Abstract]   [Full Text] [Related]  

  • 25. Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7.
    Langlois S; Yong SL; Wilson RD; Kwong LC; Kalousek DK
    J Med Genet; 1995 Nov; 32(11):871-5. PubMed ID: 8592330
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Chromosome analysis in abortion].
    Rosenkranz W; Zierler H
    Wien Med Wochenschr; 1990; 140(22):545-7. PubMed ID: 2080627
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Thrombophilia polymorphisms and intrauterine growth restriction.
    Grandone E; Margaglione M
    N Engl J Med; 2002 Nov; 347(19):1530-1; author reply 1530-1. PubMed ID: 12422894
    [No Abstract]   [Full Text] [Related]  

  • 28. Severe microcephaly with normal intellectual development: the Nijmegen breakage syndrome.
    Green AJ; Yates JR; Taylor AM; Biggs P; McGuire GM; McConville CM; Billing CJ; Barnes ND
    Arch Dis Child; 1995 Nov; 73(5):431-4. PubMed ID: 8554361
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Full trisomy 22 in a malformed newborn female.
    Feret MA; Galán F; Aguilar MS; Serrano JL; Cidras M; Garcia R
    Ann Genet; 1991; 34(1):44-6. PubMed ID: 1952793
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Possible new variant of Nijmegen breakage syndrome.
    Der Kaloustian VM; Kleijer W; Booth A; Auerbach AD; Mazer B; Elliott AM; Abish S; Usher R; Watters G; Vekemans M; Eydoux P
    Am J Med Genet; 1996 Oct; 65(1):21-6. PubMed ID: 8914736
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature.
    Brown S; Gersen S; Anyane-Yeboa K; Warburton D
    Am J Med Genet; 1993 Jan; 45(1):52-9. PubMed ID: 8418661
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pathology of intrauterine growth retardation.
    Khong TY
    Am J Reprod Immunol; 1989; 21(3-4):132-6. PubMed ID: 2701165
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetics of Silver-Russell syndrome.
    Wakeling EL; Abu-Amero S; Price SM; Stanier P; Trembath RC; Moore GE; Preece MA
    Horm Res; 1998; 49 Suppl 2():32-6. PubMed ID: 9730670
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Silver-Russell syndrome and its genetic origins.
    Rossignol S
    J Endocrinol Invest; 2006; 29(1 Suppl):9-10. PubMed ID: 16615300
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Unilateral disomy as a possible explanation for Russell-Silver syndrome.
    Hall JG
    J Med Genet; 1990 Feb; 27(2):141-2. PubMed ID: 2319587
    [No Abstract]   [Full Text] [Related]  

  • 36. Midtrimester diagnosis and anomalies in the dup(22q) syndrome: correlation of aneuploidy with low maternal serum alpha-fetoprotein and oligohydramnios.
    Johnson MP; Greb A; Goyert G; Drugan A; Qureshi F; Sacks AJ; Evans MI
    Am J Med Genet; 1990 May; 36(1):94-6. PubMed ID: 1692182
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Neonatal diabetes mellitus and microcephaly. Indications for autosomal recessive inheritance].
    Reus S; Egidi R; Otten A; Aulepp U
    Monatsschr Kinderheilkd; 1992 Nov; 140(11):803-7. PubMed ID: 1470185
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly.
    Chen CP; Chern SR; Tsai FJ; Hsu CY; Ko K; Wang W
    Taiwan J Obstet Gynecol; 2009 Sep; 48(3):323-6. PubMed ID: 19797034
    [No Abstract]   [Full Text] [Related]  

  • 39. An interstitial de-novo microdeletion of 3q26.33q27.3 causing severe intrauterine growth retardation.
    Bouman A; Weiss M; Jansen S; Hankel M; Nieuwint A; Adriaanse B; van de Kamp J; Tan-Sindhunata G
    Clin Dysmorphol; 2015 Apr; 24(2):68-74. PubMed ID: 25714561
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Mosaic trisomy 14 due to an iso dicentric chromosome (author's transl)].
    Turleau C; de Grouchy J; Cornu A; Turquet M; Millet G
    Ann Genet; 1980; 23(4):238-40. PubMed ID: 6971604
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.