• Monosomy 9p (also known as Alfi's Syndrome or simply 9P-) is a rare chromosomal disorder in which some DNA is missing or has been deleted on the short...
    11 KB (1,063 words) - 15:53, 30 March 2024
  • Progress M1-9 9p, an arm of Chromosome 9 (human) 9P/Tempel; see Tempel 1 Monosomy 9p, a chromosomal disorder due to deletion Tetrasomy 9p, a genetic disease...
    742 bytes (135 words) - 13:37, 16 January 2021
  • duplication 9q21 Chromosome 9, monosomy 9p Chromosome 9, partial monosomy 9p Chromosome 9, partial trisomy 9p Chromosome 9, tetrasomy 9p Chromosome 9, trisomy...
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  • manufacturer), a defunct German motor vehicle manufacturer Alfi's Syndrome or Monosomy 9p, a rare chromosomal disorder Alfi Conteh-Lacalle (born 1985), Spanish–Sierra...
    519 bytes (87 words) - 20:24, 4 July 2022
  • Lordosis Macrocephaly Marfan syndrome Microcephaly Micromelia Microtia Monosomy 9p Myasthenic syndrome Myelokathexis Nager's Syndrome Nail–patella syndrome...
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  • helpful with all the things the family has to face. Evan suffers from Monosomy 9p, a disease that causes skeletal abnormalities and developmental disabilities...
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  • Thumbnail for Turner syndrome
    Turner syndrome (redirect from Monosomy X)
    female is partially or completely missing an X chromosome (sex chromosome monosomy). Most people have two sex chromosomes (XX or XY). It only affects females...
    77 KB (9,090 words) - 08:13, 28 April 2024
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    HM, Leung C, Lin SP, Su YN, Su JW, Chen YT, Wang W (2012). "Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female...
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    sample since 9p is found in high concentrations in the blood. Ultrasound is another tool that may be utilized to identify tetrasomy 9p in infants prior...
    39 KB (4,295 words) - 19:58, 17 April 2024
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    clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome". Cytogenet Cell Genet. 81 (3–4): 275–7. doi:10.1159/000015045...
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  • Thumbnail for Down syndrome
    Monosomies Turner syndrome (45,X) Trisomies/tetrasomies, other karyotypes/mosaics Klinefelter syndrome (47,XXY) XXYY syndrome (48,XXYY) XXXY syndrome (48...
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  • exposure Endocrine Genetic and chromosome abnormalities Autosomal trisomy Monosomy X (45, X) Triploidy Structural abnormality of the chromosome Double or...
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    most common abnormality is monosomy of chromosome 22. Other frequent abnormalities include structural rearrangement of 1p, 3p, 9p and 6q chromosome arms.[citation...
    96 KB (10,697 words) - 06:49, 13 May 2024
  • 1:18,000-20,000 Alexander disease GFAP 1:15,600,000 Alfi's syndrome 9p monosomy 1:50,000 Alkaptonuria HGD 1:250,000-1,000,000 Alport syndrome 10q26.13...
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  • prognosis in uveal melanoma is loss of an entire copy of Chromosome 3 (Monosomy 3), which is strongly correlated with metastatic spread. Gains on chromosomes...
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  • duplication syndrome 2q31.1 microduplication Trisomy 8 Trisomy 9 Tetrasomy 9p Distal trisomy 10q Patau syndrome 13 Trisomy 16 16p11.2 duplication syndrome...
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  • Thumbnail for Birth defect
    Monosomies Turner syndrome (45,X) Trisomies/tetrasomies, other karyotypes/mosaics Klinefelter syndrome (47,XXY) XXYY syndrome (48,XXYY) XXXY syndrome (48...
    95 KB (10,067 words) - 23:46, 18 May 2024
  • Thumbnail for Miscarriage
    abnormalities found in miscarriages include an autosomal trisomy (22–32%), monosomy X (5–20%), triploidy (6–8%), tetraploidy (2–4%), or other structural chromosomal...
    111 KB (10,922 words) - 02:09, 10 May 2024
  • Monosomies Turner syndrome (45,X) Trisomies/tetrasomies, other karyotypes/mosaics Klinefelter syndrome (47,XXY) XXYY syndrome (48,XXYY) XXXY syndrome (48...
    11 KB (1,105 words) - 12:55, 17 October 2023