Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
DE DEUXCHAISNES, CHARLES NAGANT
and
KRANE, STEPHEN M.
1978.
Metabolic Bone Disease.
p.
217.
Fitch, N.
1979.
Classification and identification of inherited brachydactylies.
Journal of Medical Genetics,
Vol. 16,
Issue. 1,
p.
36.
Czeizel, A.
and
Göblyös, P.
1989.
Familial combination of brachydactyly, type E and atrial septal defect, type II.
European Journal of Pediatrics,
Vol. 149,
Issue. 2,
p.
117.
Ridgeway, Shaun
Tai, Che-Chin
and
Singh, Dishan
2004.
A Case Report of Brachydactyly Types D and E: A New Variation of Brachydactyly.
Foot & Ankle International,
Vol. 25,
Issue. 6,
p.
419.
Jensen, Kimberly
and
Hoo, Joe J.
2004.
Is brachydactyly type Ballard a variant of brachydactyly type E?.
American Journal of Medical Genetics Part A,
Vol. 129A,
Issue. 1,
p.
95.
Lu, Hong‐Yong
Cui, Ying‐Xia
Shi, Yi‐Chao
Xia, Xin‐Yi
Liang, Quan
Yao, Bing
Ge, Yi‐Feng
Li, Xiao‐Jun
and
Huang, Yu‐Feng
2009.
A girl with distinctive features of borderline high blood pressure, short stature, characteristic brachydactyly, and 11.47 Mb deletion in 12p11.21–12p12.2 by oligonucleotide array CGH.
American Journal of Medical Genetics Part A,
Vol. 149A,
Issue. 10,
p.
2321.
Kozieradzka-Ogunmakin, Iwona
2011.
Multiple epiphyseal dysplasia in an Old Kingdom Egyptian skeleton: A case report.
International Journal of Paleopathology,
Vol. 1,
Issue. 3-4,
p.
200.
Fraser, Michael R.
and
Sechriest, V. Franklin
2011.
Total Knee Arthroplasty in a Patient With Pseudopseudohypoparathyroidism.
Orthopedics,
Vol. 34,
Issue. 8,
Pereda, Arrate
Garin, Intza
Garcia-Barcina, Maria
Gener, Blanca
Beristain, Elena
Ibañez, Ane Miren
and
Perez de Nanclares, Guiomar
2013.
Brachydactyly E: isolated or as a feature of a syndrome.
Orphanet Journal of Rare Diseases,
Vol. 8,
Issue. 1,
Wang, Jian
Wang, Zhigang
An, Yu
Wu, Chunxing
Xu, Yunlan
Fu, Qihua
Shen, Yiping
and
Zhang, Qinghua
2015.
Exome sequencing reveals a novel PTHLH mutation in a Chinese pedigree with brachydactyly type E and short stature.
Clinica Chimica Acta,
Vol. 446,
Issue. ,
p.
9.
Jamsheer, Aleksander
Sowińska-Seidler, Anna
Olech, Ewelina M
Socha, Magdalena
Kozłowski, Kazimierz
Pyrkosz, Antoni
Trzeciak, Tomasz
Materna-Kiryluk, Anna
and
Latos-Bieleńska, Anna
2016.
Variable expressivity of the phenotype in two families with brachydactyly type E, craniofacial dysmorphism, short stature and delayed bone age caused by novel heterozygous mutations in the PTHLH gene.
Journal of Human Genetics,
Vol. 61,
Issue. 5,
p.
457.
Bae, Jihong
Choi, Hong Seok
Park, So Young
Lee, Do-Eun
and
Lee, Sihoon
2018.
Novel Mutation inPTHLHRelated to Brachydactyly Type E2 Initially Confused with Unclassical Pseudopseudohypoparathyroidism.
Endocrinology and Metabolism,
Vol. 33,
Issue. 2,
p.
252.
Huang, Jia
Liu, Hong-Yan
Wang, Rong-Rong
Xiao, Hai
Wu, Dong
Li, Tao
Jiang, Ying-Hai
and
Zhang, Xue
2019.
A 3.06-Mb interstitial deletion on 12p11.22-12.1 caused brachydactyly type E combined with pectus carinatum.
Chinese Medical Journal,
Vol. 132,
Issue. 14,
p.
1681.
Dorado, Enrique
Herrerín, Jesús
Ramírez, Ildefonso
Parro, Loreto
Carrillo, Manuel F.
and
Murillo, Jorge
2021.
A case of brachymetacarpia in a skeleton from a Mudejar cemetery from Spain (13th–14th century AD).
International Journal of Osteoarchaeology,
Vol. 31,
Issue. 4,
p.
621.
Manouvrier-Hanu, S.
Petit, F.
and
Mezel, A.
2023.
Clasificación de las malformaciones congénitas de los miembros.
EMC - Aparato Locomotor,
Vol. 56,
Issue. 4,
p.
1.
Ivanovich, Zavarukhin V.
2023.
Pediatric Hand Surgery.
p.
139.
Sun, Jian
Yang, Nian
Xu, Zhengquan
Cheng, Hongbo
and
Zhang, Xiangxin
2024.
A novel heterozygous mutation in PTHLH causing autosomal dominant brachydactyly type E complicated with short stature.
Molecular Genetics & Genomic Medicine,
Vol. 12,
Issue. 2,