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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1912 1
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1952 5
1953 9
1954 6
1955 4
1956 4
1957 3
1958 1
1959 2
1960 1
1961 1
1962 2
1963 2
1964 2
1965 1
1966 2
1967 8
1968 5
1969 12
1970 4
1971 9
1972 11
1973 9
1974 5
1975 8
1976 13
1977 10
1978 14
1979 5
1980 5
1981 4
1982 4
1983 11
1984 17
1985 10
1986 11
1987 4
1988 8
1989 8
1990 4
1991 10
1992 14
1993 19
1994 15
1995 18
1996 17
1997 22
1998 17
1999 27
2000 18
2001 34
2002 30
2003 28
2004 31
2005 31
2006 43
2007 34
2008 38
2009 35
2010 43
2011 48
2012 34
2013 37
2014 40
2015 45
2016 38
2017 48
2018 35
2019 39
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1,341 results

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Page 1
Grebe syndrome.
Saminathan D. Saminathan D. Indian Pediatr. 2010 Sep;47(9):791. Indian Pediatr. 2010. PMID: 21048264 Free article. No abstract available.
[Grebe syndrome].
Ieshima A. Ieshima A. Ryoikibetsu Shokogun Shirizu. 2001;(33):769-70. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462677 Review. Japanese. No abstract available.
Comparative analysis of the gut bacteria of the relict gull (Larus Relictus) and black-necked grebe (Podiceps Nigricollis) in Erdos Relic Gull National Nature Reserve in Inner Mongolia, China.
Zhao Y, Bao D, Sun Y, Meng Y, Li Z, Liu R, Lang J, Liu L, Gao L. Zhao Y, et al. PeerJ. 2023 Jul 10;11:e15462. doi: 10.7717/peerj.15462. eCollection 2023. PeerJ. 2023. PMID: 37456862 Free PMC article.
The prominent phylum in the relict gull was Proteobacteria, whereas the prominent phylum in the black-necked grebe was Firmicutes. The average relative abundance of the 17 genera identified was greater than 1%. The dominant genus in the relict gull was Escherichia-Shigella …
The prominent phylum in the relict gull was Proteobacteria, whereas the prominent phylum in the black-necked grebe was Firmicutes. Th …
A novel variant in BMPR1B causes acromesomelic dysplasia Grebe type in a consanguineous Moroccan family: Expanding the phenotypic and mutational spectrum of acromesomelic dysplasias.
Lhousni S, Charif M, Derouich Y, Elidrissi Errahhali M, Elidrissi Errahhali M, Ouarzane M, Lenaers G, Boulouiz R, Belahcen M, Bellaoui M. Lhousni S, et al. Bone. 2023 Oct;175:116860. doi: 10.1016/j.bone.2023.116860. Epub 2023 Jul 29. Bone. 2023. PMID: 37524292
Acromesomelic dysplasia Grebe type (AMD Grebe type) is an autosomal recessive trait characterized by short stature, shortened limbs and malformations of the hands and feet. ...Here, we report a novel homozygous BMPR1B variant causing AMD Grebe type in a consa …
Acromesomelic dysplasia Grebe type (AMD Grebe type) is an autosomal recessive trait characterized by short stature, shortened …
A GDF5 frameshift mutation segregating with Grebe type chondrodysplasia and brachydactyly type C+ in a 6 generations family: Clinical report and mini review.
Faryal S, Farooq M, Abdullah U, Ali Z, Saadi SM, Ullah F, Khan K, Sarwar Y, Sher M, Chopra AA, Tommerup N, Baig SM. Faryal S, et al. Eur J Med Genet. 2021 Jul;64(7):104226. doi: 10.1016/j.ejmg.2021.104226. Epub 2021 Apr 16. Eur J Med Genet. 2021. PMID: 33872773 Review.
Different mutations in the Growth/Differentiation Factor 5 gene (GDF5) have been associated with varying types of skeletal dysplasia, including Grebe type chondrodysplasia (GTC), Hunter-Thompson syndrome, Du Pan Syndrome and Brachydactyly type C (BDC). ...
Different mutations in the Growth/Differentiation Factor 5 gene (GDF5) have been associated with varying types of skeletal dysplasia, includ …
Grebe dysplasia and the spectrum of CDMP1 mutations.
Stelzer C, Winterpacht A, Spranger J, Zabel B. Stelzer C, et al. Pediatr Pathol Mol Med. 2003 Jan-Feb;22(1):77-85. doi: 10.1080/pdp.22.1.77.85. Pediatr Pathol Mol Med. 2003. PMID: 12687891
We report on a 4-year-old boy with the typical phenotype of Grebe dysplasia born to consanguineous parents. The father seems to be unaffected; the mother presents with brachydactyly type C (BdC). ...A dominant negative action on other bone morphogenetic proteins is unlikel …
We report on a 4-year-old boy with the typical phenotype of Grebe dysplasia born to consanguineous parents. The father seems to be un …
Aufbruch ins Pharmatasialand.
Grebe I. Grebe I. CME (Berl). 2023;20(6):44-45. doi: 10.1007/s11298-023-3215-7. Epub 2023 Jun 9. CME (Berl). 2023. PMID: 37325235 Free PMC article. German. No abstract available.
In Reply.
Hines J, Bancos I, Grebe SKG, Singh RJ. Hines J, et al. Clin Chem. 2018 Aug;64(8):1258-1259. doi: 10.1373/clinchem.2018.290205. Epub 2018 May 30. Clin Chem. 2018. PMID: 29848546 No abstract available.
Grebe dysplasia - prenatal diagnosis based on rendered 3-D ultrasound images of fetal limbs.
Goncalves LF, Berger JA, Macknis JK, Bauer ST, Bloom DA. Goncalves LF, et al. Pediatr Radiol. 2017 Jan;47(1):108-112. doi: 10.1007/s00247-016-3705-9. Epub 2016 Sep 27. Pediatr Radiol. 2017. PMID: 27677752
Grebe dysplasia is a rare skeletal dysplasia characterized by severe acromesomelic shortening of the long bones in a proximal to distal gradient of severity, with bones of the hands and feet more severely affected than those of the forearms and legs, which in turn are more …
Grebe dysplasia is a rare skeletal dysplasia characterized by severe acromesomelic shortening of the long bones in a proximal to dist …
Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia.
Faiyaz-Ul-Haque M, Ahmad W, Wahab A, Haque S, Azim AC, Zaidi SH, Teebi AS, Ahmad M, Cohn DH, Siddique T, Tsui LC. Faiyaz-Ul-Haque M, et al. Am J Med Genet. 2002 Jul 22;111(1):31-7. doi: 10.1002/ajmg.10501. Am J Med Genet. 2002. PMID: 12124730 Review.
Grebe-type chondrodysplasia exhibits a severe form of limb shortening and appendicular bone dysmorphogenesis. ...
Grebe-type chondrodysplasia exhibits a severe form of limb shortening and appendicular bone dysmorphogenesis. ...
1,341 results