Search Results

Griscelli syndrome type 3 in Ethiopian sisters resulting from a homozygous missense mutation in MLPH.

• Authors : Dagnewu, Kidist Y. (AUTHOR); Ayele, Adane (AUTHOR); Liu, Lu (AUTHOR)

Subjects: MISSENSE mutation; SISTERS; SYNDROMES

• Source: International Journal of Dermatology. Mar2020, Vol. 59 Issue 3, pe55-e57. 3p. 1 Color Photograph, 1 Diagram.

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Greater understanding about a rare inherited skin disorder from a study of NLRP1 in two sisters with different severity of disease.

Subjects: SISTERS

• Source: British Journal of Dermatology. Feb2023, Vol. 188 Issue 2, pe18-e18. 1p.

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CHANGING ATTITUDES, CHANGING LIVES.

• Authors : SHRIVER, EUNICE KENNEDY

Subjects: PEOPLE with intellectual disabilities; INTELLECTUAL disabilities; SISTERS

• Source: Saturday Evening Post. Jan/Feb2019, Vol. 291 Issue 1, p55-55. 1p.

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Novel compound heterozygous FATP4 mutations caused ichthyosis prematurity syndrome in Spanish sisters.

• Authors : Esperón‐Moldes, Uxía Saraiva; Ginarte, Manuel; Santamariña, Marta

Subjects: ICHTHYOSIS; PALMOPLANTAR keratoderma; SISTERS

• Source: Acta Paediatrica. Apr2019, Vol. 108 Issue 4, p763-765. 3p.

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Friedreich’s ataxia: clinical heterogeneity in two sisters.

• Authors : Armani, M.; Zortea, M.; Pastorello, E.

Subjects: ATAXIA; TENDONS; PHENOTYPES

• Source: Neurological Sciences. Jun2006, Vol. 27 Issue 2, p140-142. 3p.

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Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness.

• Authors : Robitaille, Pierre; Merouani, Aicha; He, Ning

Subjects: BARTTER syndrome; HYPERALDOSTERONISM; GENETIC mutation

• Source: European Journal of Pediatrics. Sep2011, Vol. 170 Issue 9, p1209-1211. 3p. 1 Graph.

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JOHNSON & JOHNSON.

• Authors : McGlashan, Lara

Subjects: JOHNSON, Tanji; JOHNSON, Safiya; WEIGHT training

• Source: Joe Weider's Muscle & Fitness. Jan2007, Vol. 68 Issue 1, p200-206. 6p. 10 Color Photographs, 3 Charts.

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My Sister, My Guide.

• Authors : Walsh, Jennifer

Subjects: SISTERS; COGNITION

• Source: Women's Health. Mar2018, Vol. 15 Issue 2, p104-104. 1p. 4 Color Photographs.

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A novel P1PK allele in two Bangladeshi sisters with a history of spontaneous abortion: A4GALT*02N(951C).

• Authors : Floch, Aline (AUTHOR); Lomas‐Francis, Christine (AUTHOR); Vege, Sunitha (AUTHOR)

Subjects: MISCARRIAGE; RECURRENT miscarriage; ALLELES

• Source: Transfusion. Oct2021, Vol. 61 Issue 10, pE71-E72. 2p.

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reality check.

• Authors : Millner, Denene

Subjects: PARENTING; BASHFULNESS in children; FRIENDSHIP

• Source: Parenting. Nov2006, Vol. 20 Issue 10, p55-57. 2p. 2 Color Photographs.

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